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1.

図書

図書
edited by Manfred Schlosser
出版情報: Chichester : J. Wiley, c2002  x, 1243 p. ; 26 cm
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List of Contributors
Preface to the First Edition
Preface to the Second Edition
Organoalkali Chemistry / Manfred SchlosserI:
Organotin Chemistry / James A. MarshallII:
Organoboron Chemistry / Keith SmithIII:
Organoaluminum Chemistry / Hisashi YamamotoIV:
Organozinc Chemistry / Eiichi NakamuraV:
Organocopper Chemistry / Bruce H. LipshutzVI:
Organotitanium Chemistry / Manfred T. ReetzVII:
Organozirconium Chemistry / Ei-ichi NegishiVIII:
Organoiron and Organochromium Chemistry / Martin F. SemmelhackIX:
Organopalladium Chemistry / Louis S. HegedusX:
Index
List of Contributors
Preface to the First Edition
Preface to the Second Edition
2.

図書

図書
by László Kürti and Barbara Czakó ; [foreword by E.J. Corey] ; [introduction by K.C. Nicolaou]
出版情報: Amsterdam ; Tokyo : Elsevier, c2005  lii, 758 p. ; 28 cm
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Foreword / E.J. CoreyI:
Introduction / K.C. NicolaouII:
Preface / III:
Explanation of the Use of Colors in the Schemes and Text / IV:
List of Abbreviations / V:
List of Named Organic Reactions / VI:
Named Organic Reactions in Alphabetical Order / VII:
Appendix: Listing of the Named Reactions by Synthetic Type and by their Utility / VIII:
Brief explanation of the organization of this section / 8.1:
List of named reactions in chronological order of their discovery / 8.2:
Reaction categories - Categorization of named reactions in tabular format / 8.3:
Affected functional groups - Listing of transformations in tabular format / 8.4:
Preparation of functional groups - Listing of transformations in tabular format / 8.5:
References / IX:
Index / X:
Foreword / E.J. CoreyI:
Introduction / K.C. NicolaouII:
Preface / III:
3.

図書

図書
edited by Kevin Burgess
出版情報: New York : Wiley-Interscience, c2000  xiv, 277 p. ; 24 cm
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Preface
Contributors
Solid-Phase Syntheses of Guanidines / Kevin Burgess ; Jiong Chen1:
Introduction / 1.1.:
Outline of Some Solution-Phase Approaches to Guanidines / 1.2.:
Solid-Phase Syntheses Involving Resin-Bound Electrophiles / 1.3.:
Solid-Phase Syntheses Involving Electrophiles in Solution / 1.4.:
Other Supported Guanidines / 1.5.:
Conclusion / 1.6.:
References
Palladium-Catalyzed Carbon-Carbon Bond Formation on Solid Support / Matthew H. Todd ; Chris Abell2:
Heck Reaction / 2.1.:
Stille Reaction / 2.3.:
Suzuki Reaction / 2.4.:
Miscellaneous Reactions / 2.5.:
Concluding Remarks / 2.6.:
Benzofused Heterocycles Via Solid-Phase S[subscript N]AR Reactions / Matthias K. Schwarz ; Mark A. Gallop3:
Formation of [6,7]- and [6,8]-Fused Systems / 3.1.:
Formation of [6,6]-Fused Systems / 3.3.:
Formation of [6,5]-Fused Systems / 3.4.:
Conclusions and Outlook / 3.5.:
Solid-Phase Synthesis of Sequence-Specific Phenylacetylene Oligomers / Jeffrey S. Moore ; David J. Hill ; Matthew J. Mio4:
Strategies / 4.1.:
Synthetic Tactics / 4.3.:
Illustrative Applications / 4.4.:
Scope and Limitations / 4.5.:
Representative Procedures / 4.6.:
Polymer-Assisted Solution-Phase Methods for Chemical Library Synthesis / Daniel L. Flynn ; Rajesh V. Devraj ; John J. Parlow5:
Reactant Sequestration / 5.1.:
Byproduct Sequestration / 5.3.:
Solution-Phase Derivatization to Facilitate Polymer-Assisted Sequestration / 5.4.:
Soluble Bifunctional Reagents / 5.5.:
Polymer-Supported Substrates / 5.6.:
Polymer-Supported Reagents / 5.7.:
Polymer-Supported Catalysts / 5.8.:
Polymers for Reaction Quenching/Workup / 5.9.:
Combinations of Solid- and Solution-Phase Techniques in Organic Synthesis / 5.10.:
Multistep/One-Chamber Solution-Phase Synthesis / 5.11.:
Polymer-Assisted Technologies in Multistep Solution-Phase Syntheses / 5.12.:
Solid-Phase Organic Synthesis on Radiation-Grafted Polymer Surfaces: Application of Synphase Crowns to Multiple Parallel Syntheses / Ian W. James ; Geoffrey Wickham ; Nicholas J. Ede ; Andrew M. Bray5.13.:
Multiple Parallel Syntheses of Individual Compounds / 6.1.:
Synthetic Applications of Synphase Crowns / 6.2.:
Linker Development Using Synphase Crowns / 6.3.:
Tagging Methods for Identifying Individual Crowns / 6.4.:
Future Developments / 6.5.:
Vibrational Spectroscopy for Optimization of Solid-Phase Organic Syntheses / Bing Yan7:
Spectroscopic Methods Applicable to Different Sample Sizes / 7.1.:
Optimization in Solid-Phase Organic Syntheses / 7.3.:
Recent Advances in Solid-Phase Synthesis of Natural Products / Lawrence J. Wilson7.4.:
Prostaglandins / 8.1.:
Epothilone a / 8.3.:
(S)-Zearalenone / 8.4.:
DL-Muscone / 8.5.:
Taxoid Libraries from Baccatin III / 8.6.:
Sarcodictyin Libraries / 8.7.:
Lavendustin A / 8.8.:
Indolyl Diketopiperazines / 8.9.:
Balanol Analogs / 8.10.:
Pseudoalkaloids from Shikimic Acid / 8.11.:
Conclusions / 8.12.:
Index
Preface
Contributors
Solid-Phase Syntheses of Guanidines / Kevin Burgess ; Jiong Chen1:
4.

図書

図書
volume editor, S. Kobayashi ; with contributions by R. Anwander [et al.]
出版情報: New York ; Tokyo : Springer, c1999  305 p. ; 24 cm
シリーズ名: Topics in organometallic chemistry ; 2
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5.

図書

図書
Garry Procter
出版情報: Oxford : Oxford University Press, 1998  89 p. ; 25 cm
シリーズ名: Oxford chemistry primers ; 63
Oxford science publications
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Introduction / 1:
Stereochemistry of reactions / 2:
Additions to carbonyl compounds / 3:
Reactions of enolates / 4:
Aldol reactions / 5:
Additions to double bonds / 6:
Reduction / 7:
Oxidation / 8:
Rearrangements / 9:
Hydrolysis and esterification / 10:
Answers to problems
Index
Introduction / 1:
Stereochemistry of reactions / 2:
Additions to carbonyl compounds / 3:
6.

図書

図書
edited by Stanley M. Roberts, John Whittall
出版情報: Chichester : J. Wiley & Sons, c2007  xxii, 312 p. ; 24 cm
シリーズ名: Catalysts for fine chemical synthesis ; v. 5
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Series Preface
Preface to Volume 5
Abbreviations
Industrial Catalysts for Regio- or Stereo-Selective Oxidations and Reductions A Review of Key Technologies and Targets / John Whittall1:
Introduction / 1.1:
Reduction of Carbon-Carbon Double Bonds / 1.2:
Privileged structures: [alpha]-amino acids and itaconic acids / 1.2.1:
[beta]-Amino acids / 1.2.2:
[alpha]-Alkyl substituted acids / 1.2.3:
[alpha]-Alkoxy substituted acids / 1.2.4:
Unsaturated nitriles / 1.2.5:
Alkenes and allyl alcohols / 1.2.6:
[alpha],[beta]-Unsaturated aldehyde reduction / 1.2.7:
Ketone and Imine Reduction / 1.3:
Catalytic hydrogenation of ketones and imines / 1.3.1:
Asymmetric transfer hydrogenation (ATH) catalysts / 1.3.2:
Modified borane reagents / 1.3.3:
Biocatalysts (alcohol dehydrogenases and ketoreductases) / 1.3.4:
Oxidation / 1.4:
Sharpless chiral epoxidation of allyl alcohols / 1.4.1:
Dioxirane catalyzed epoxidation / 1.4.2:
Amines and iminium salts / 1.4.3:
Phase transfer catalysts / 1.4.4:
The Julia-Colonna method (polyleucine oxidation) / 1.4.5:
Organocatalytic [alpha]-hydroxylation of ketones / 1.4.6:
Baeyer-Villiger oxidation / 1.4.7:
Chiral sulfoxides / 1.4.8:
References
Asymmetric Hydrogenation of Alkenes, Enones, Ene-Esters and Ene-Acids / 2:
(S)-2,2[prime]-Bis{[di(4-methoxyphenyl)phosphinyl]oxy}-5,5[prime],6,6[prime],7,7[prime],8,8[prime]-octahydro-1,1[prime]-binaphthyl as a ligand for rhodium-catalyzed asymmetric hydrogenation / Ildiko Gergely ; Csaba Hegedus ; Jozsef Bakos2.1:
Synthesis of (S)-5,5[prime],6,6[prime],7,7[prime],8,8[prime]-Octahydro-1,1[prime]-bi-2-naphthol / 2.1.1:
Synthesis of (S)-2,2[prime]-Bis{[di(4-methoxyphenyl)phosphinyl]oxy}-5,5[prime],6,6[prime],7,7[prime],8,8[prime]-octahydro-1,1[prime]-binaphthyl / 2.1.2:
Asymmetric hydrogenation of Dimethyl itaconate / 2.1.3:
Conclusion
Synthesis and application of phosphinite oxazoline iridium complexes for the asymmetric hydrogenation of alkenes / Frederik Menges ; Andreas Pfaltz2.2:
Synthesis of (4S,5S)-2-(5-Methyl-2-phenyl-4,5-dihydro-oxazol-4-yl)-1,3-diphenyl-propan-2-ol / 2.2.1:
Synthesis of (4S,5S)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydro-oxazol-4-yl)-2-phenyl-ethyl]-diphenylphosphinite / 2.2.2:
Synthesis of (4S,5S)-[([eta superscript 4]-1,5-Cyclooctadiene)-{2-(2-phenyl-5-methyl-4,5-dihydro-oxazol-4-yl)-1,3-diphenyl-2-diphenylphosphinite-propane}iridium(I)]-tetrakis[3,5-bis(trifluoromethyl)phenyl]borate / 2.2.3:
Asymmetric hydrogenation of trans-[alpha]-Methylstilbene / 2.2.4:
Synthesis and application of heterocyclic phosphine oxazoline (HetPHOX) iridium complexes for the asymmetric hydrogenation of alkenes / Pier Giorgio Cozzi2.3:
Synthesis of (4S)-tert-Butyl-2-(thiophene-2-yl)-4,5-dihydrooxazole / 2.3.1:
Synthesis of (4S)-tert-Butyl-2-(3-diphenylphosphino-thiophene-2-yl)-4,5-dihydrooxazole / 2.3.2:
Synthesis of (4S)-[([eta superscript 4]-1,5-Cyclooctadiene)-{4-tert-butyl-2-(3-diphenylphosphino-thiophene-2-yl)-4,5-dihydrooxazole}iridium(I)]-tetrakis [3,5-bis(trifluoromethyl)phenyl]borate / 2.3.3:
(R)-2,2[prime],6,6[prime]-Tetramethoxy-bis[di(3,5-dimethylphenyl)phosphino]-3,3[prime]-bipyridine [(R)-Xyl-P-Phos] as a ligand for rhodium-catalyzed asymmetric hydrogenation of [alpha]-dehydroamino acids / Jing Wu ; Albert S.C. Chan2.3.4:
Synthesis of 3-Bromo-2,6-dimethoxypyridine / 2.4.1:
Synthesis of Bis(3,5-dimethylphenyl)phosphine chloride / 2.4.2:
Synthesis of 3-Bromo-2,6-dimethoxy-4-di(3,5-dimethylphenyl)phosphinopyridine / 2.4.3:
2,2[prime],6,6[prime]-Tetramethoxy-bis[di(3,5-dimethylphenyl)phosphinoyl]-3,3[prime]-bipyridine / 2.4.4:
Optical resolution of ([plus or minus])-6 with (-) or (+)-2,3-0,0[prime]-Dibenzoyltartaric acid monohydrate [(R)-6 or (S)-6)] / 2.4.6:
(R)-2,2[prime],6,6[prime]-Tetramethoxy-bis[di(3,5-dimethylphenyl)phosphino]-3,3[prime]-bipyridine [(R)-Xyl-P-Phos, (R)-1] / 2.4.7:
Preparation of the stock solution of [Rh(R-Xyl-P-Phos)(COD)]BF[subscript 4] / 2.4.8:
A typical procedure for the asymmetric hydrogenation of methyl (Z)-2-Acetamidocinnamate / 2.4.9:
(R,R)-2,3-Bis(tert-butylmethylphosphino)quinoxaline (QuinoXP) as a ligand for rhodium-catalyzed asymmetric hydrogenation of prochiral amino acid and amine derivatives / Tsuneo Imamoto ; Aya Koide2.5:
Synthesis of (R)-tert-Butyl(hydroxymethyl)methylphosphine-borane / 2.5.1:
Synthesis of (R)-Benzoyloxy(tert-butyl)methylphosphine-borane / 2.5.2:
Synthesis of (S)-tert-Butylmethylphosphine-borane / 2.5.3:
(R,R)-2,3-Bis(tert-butylmethylphosphino)quinoxaline (QuinoxP) / 2.5.4:
Asymmetric hydrogenation of Methyl (E)-3-acetylamino-2-butenoate catalyzed by Rh(I)-(R,R)-2,3-Bis(tert-butylmethylphosphino)quinoxaline / 2.5.5:
Rhodium-catalyzed asymmetric hydrogenation of indoles / Ryoichi Kuwano ; Masaya Sawamura2.6:
Synthesis of (R)-2-[(S)-1-(Dimethylamino)ethyl]-1-iodoferrocene / 2.6.1:
Synthesis of (R)-2-[(S)-1-(Diphenylphosphinyl)ethyl]-1-iodoferrocene / 2.6.2:
Synthesis of (R,R)-2,2[prime]-Bis[(S)-1-(diphenylphosphinyl)ethyl]-1,1[Prime]-biferrocene / 2.6.3:
Synthesis of (R,R)-2,2[Prime]-Bis[(S)-1-(diphenylphosphino)ethyl]-1,1[Prime]-biferrocene [abbreviated to (S,S)-(R,R)-PhTRAP] / 2.6.4:
Catalytic asymmetric hydrogenation of N-Acetyl-2-butylindole / 2.6.5:
Catalytic asymmetric hydrogenation of 3-Methyl-N-(p-toluenesulfonyl)indole / 2.6.6:
Asymmetric Reduction of Ketones / 3:
(R,R)-Bis(diphenylphosphino)-1,3-diphenylpropane as a versatile ligand for enantioselective hydrogenations / Natalia Dubrovina ; Armin Borner3.1:
Synthesis of (S,S)-1,3-Diphenylpropane-1,3-diol / 3.1.1:
Synthesis of (S,S)-Methanesulfonyloxy-1,3-diphenylpropane-1,3-diol / 3.1.2:
Synthesis of (R,R)-Bis(diphenylphosphino)-1,3-diphenylpropane / 3.1.3:
Synthesis of both enantiomers of 1-Phenylethanol by reduction of acetophenone with Geotrichum candidum IFO 5767 / Kaoru Nakamura ; Mikio Fujii ; Yoshiteru Ida3.2:
Cultivation of G. candidum IFO 5767 / 3.2.1:
Synthesis of (S)-1-Phenylethanol / 3.2.2:
Synthesis of (R)-1-Phenylethanol / 3.2.3:
Titanocene-catalyzed reduction of ketones in the presence of water. A convenient procedure for the synthesis of alcohols via free-radical chemistry / Antonio Rosales ; Juan M. Cuerva ; J. Enrique Oltra3.3:
Titanocene-catalyzed reduction of Acetophenone in the presence of water / 3.3.1:
Titanocene-catalyzed synthesis of Methyl 4-deuterio-4-phenyl-4-hydroxybutanoate / 3.3.2:
Xyl-tetraPHEMP: a highly efficient biaryl ligand in the [diphosphine RuCl[subscript 2] diamine]-catalyzed hydrogenation of simple aromatic ketones / Paul H. Moran ; Julian P. Henschke ; Antonio Zanotti-Gerosa ; Ian C. Lennon3.4:
Synthesis of Tri(3,5-dimethylphenyl)phosphine oxide / 3.4.1:
Synthesis of Bis(3,5-dimethylphenyl)-(2-iodo-3,5-dimethylphenyl)phosphine oxide / 3.4.2:
Synthesis of rac-4,4[prime],6,6[prime]-Tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphinoyl]-biphenyl / 3.4.3:
Synthesis of rac-4,4[prime],6,6[prime]-Tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphino]-biphenyl [abbreviated to (rac)-Xyl-tetraPHEMP] / 3.4.4:
Synthesis of [(R)-N,N-Dimethyl(1-methyl)benzylaminato-C[superscript 2],N]-{rac-4,4[prime],6,6[prime]-tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphino]-biphenyl}-palladium(II) tetrafluoroborate and separation of the diastereomers / 3.4.5:
Synthesis of (S)-4,4[prime],6,6[prime]-Tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphino]-biphenyl: [abbreviated to (S)-Xyl-tetraPHEMP) and (R)-4,4[prime],6,6[prime]-Tetramethyl-2,2[prime]-bis[bis(3,5-dimethylphenyl)phosphino]-biphenyl [abbreviated to (R)-Xyl-tetraPHEMP] / 3.4.6:
Synthesis of [(R)-Xyl-tetraPHEMP RuCl[subscript 2] (R,R)-DPEN] and [(S)-Xyl-tetraPHEMP RuCl[subscript 2] (S,S)-DPEN] / 3.4.7:
Reduction of Acetophenone using [(S)-Xyl-tetraPHEMP RuCl[subscript 2] (S,S)-DPEN] as a precatalyst / 3.4.8:
N-Arenesulfonyl- and N-Alkylsulfamoyl-1,2-diphenylethylenediamine ligands for ruthenium-catalyzed asymmetric transfer hydrogenation of activated ketones / Michel (Massoud S.) Stephan ; Barbara Mohar3.5:
Synthesis of N-Arenesulfonyl-1,2-diphenylethylenediamines / 3.5.1:
Preparation of Ru(II)-N-arenesulfonyl-1,2-diphenylethylenediamine complexes / 3.5.2:
Asymmetric transfer hydrogenation of Ethyl benzoylacetate / 3.5.3:
The synthesis and application of BrXuPHOS: a novel monodentate phosphorus ligand for the asymmetric hydrogenation of ketones / Martin Wills ; Yingjian Xu ; Garden Docherty ; Gary Woodward3.6:
Synthesis of (S)-BrXuPHOS / 3.6.1:
Synthesis of (S,S,SS)-BrXuPHOS-Ru-DPEN / 3.6.2:
General procedure of asymmetric hydrogenation of acetophenone / 3.6.3:
Acknowledgement
In Situ formation of ligand and catalyst: application in ruthenium-catalyzed enantioselective reduction of ketones / Jenny Wettergren ; Hans Adolfsson3.7:
Synthesis of (S)-3-Fluoro-1-phenylethanol / 3.7.1:
Synphos and Difluorphos as ligands for ruthenium-catalyzed hydrogenation of alkenes and ketones / Severine Jeulin ; Virginie Ratovelomanana-Vidal ; Jean-Pierre Genet3.8:
Synthesis of [RuCl((S)-SYNPHOS)(p-cymene)]Cl / 3.8.1:
Synthesis of [RuCl((S)-DIFLUORPHOS)(p-cymene)]Cl / 3.8.2:
Synthesis of [RuI((S)-DIFLUORPHOS)(p-cymene)]I / 3.8.3:
Synthesis of [NH[subscript 2]R[subscript 2]] [(RuCl(PP))[subscript 2]([Mu]-Cl)[subscript 3]] PP = SYNPHOS or DIFLUORPHOS and R = Me or Et / 3.8.4:
Synthesis of [NH[subscript 2]Me[subscript 2]][RuCl-(S)-DIFLUORPHOS][subscript 2][[Mu]-Cl][subscript 3] / 3.8.5:
Synthesis of in situ generated [RuBr[subscript 2]((S)-SYNPHOS)] and [RuBr[subscript 2]((S)-DIFLUORPHOS)] / 3.8.6:
An arene ruthenium complex with polymerizable side chains for the synthesis of immobilized catalysts / Estelle Burri ; Silke B. Wendicke ; Kay Severin3.9:
Synthesis of 2-Methyl-cyclohexa-2,5-dienecarboxylic acid 2-(2-methyl-acryloyloxy)-ethyl ester / 3.9.1:
Synthesis of [[eta superscript 6]-(2-Methyl-benzoic acid 2-(2-methyl-acryloyloxy)-ethyl ester)RuCl[subscript 2]][subscript 2] / 3.9.2:
Selective reduction of carbonyl group in [beta], [gamma]-unsaturated [alpha]-alpha-ketoesters by transfer hydrogenation with Ru-(p-cymene) (TsDPEN) / Minjie Guo ; Dao Li ; Yanhui Sun ; Zhaoguo Zhang3.10:
Synthesis of Di-[Mu]-chloro-bis[chloro([eta superscript 6]-1-isopropyl-4-methyl-benzene)ruthenium(II) / 3.10.1:
Synthesis of ([plus or minus])-Monotosylate-1,2-diphenyl-1,2-ethylenediamine / 3.10.2:
Synthesis of Ru complex Ru(p-cymene)(TsDPEN) / 3.10.3:
Ru-TsDPEN catalyzed transfer hydrogenation reaction of [beta],[gamma]-unsaturated-[alpha]-ketoesters / 3.10.4:
Preparation of polymer-supported Ru-TsDPEN catalysts and their use for the enantioselective synthesis of (S)-fluoxetine / Liting Chai ; Yangzhou Li ; Quanrui Wang3.11:
Synthesis of the supported ligand 9 / 3.11.1:
Synthesis of ligand 17 / 3.11.2:
General procedure for asymmetric transfer hydrogenation / 3.11.3:
Preparation of (S)-Fluoxetine hydrochloride / 3.11.4:
Polymer-supported chiral sulfonamide-catalyzed reduction of [beta]-keto nitriles: a practical synthesis of (R)-Fluoxetine / Guang-yin Wang ; Gang Zhao3.12:
Synthesis of (R)-3-Amino-1-phenyl-propan-1-ol / 3.12.1:
Synthesis of (R)-ethyl 3-hydroxy-3-phenylpropylcarbamate / 3.12.2:
Synthesis of (R)-3-(Methylamino)-1-phenylpropan-1-ol / 3.12.3:
Synthesis of (R)-Fluoxetine / 3.12.4:
Imine Reduction and Reductive Amination / 4:
Metal-free reduction of imines: enantioselective Bronsted acid-catalyzed transfer hydrogenation using chiral BINOL-phosphates as catalysts / Magnus Rueping ; Erli Sugiono ; Cengiz Azap ; Thomas Theissmann4.1:
Synthesis of (R)-2,2[prime]-Bis-methoxymethoxy-[1,1[prime]] binaphthalene (MOM-BINOL) / 4.1.1:
Synthesis of (R)-3,3[prime]-Diiodo-2,2[prime]-bis(methoxymethoxy)-1,1[prime]-binaphthalene / 4.1.2:
Synthesis of 3,3[prime]-Bis-(3,5[prime]-bis-trifluoromethyl-phenyl)-2,2[prime]-bismethoxymethoxy [1,1[prime]-binaphthalene] / 4.1.3:
Synthesis of (R)-3,3[prime]-[3,5-Bis(trifluoromethyl)phenyl]-1,1[prime]-binaphthylphosphate / 4.1.4:
General procedure for the transfer hydrogenation of ketimines / 4.1.5:
Synthesis of [1-(2,4-Dimethyl-phenyl)-ethyl]-(4-methoxy-phenyl)-amine / 4.1.6:
Metal-free Bronsted acid-catalyzed transfer hydrogenation: enantioselective synthesis of tetrahydroquinolines / Andrey P. Antonchick4.2:
General procedure for the transfer hydrogenation of quinolines / 4.2.1:
Synthesis of 7-Chloro-4-phenyl-1,2,3,4-tetrahydroquinoline / 4.2.2:
Synthesis of (S)-2-Phenyl-1,2,3,4-tetrahydroquinoline / 4.2.3:
Synthesis of (R)-2-(2-(Benzo[1,3]dioxol-5-yl)ethyl)-1,2.3,4-tetrahydro-quinoline / 4.2.4:
A highly stereoselective synthesis of 3[alpha]-Amino-23,24-bisnor-5[alpha]-cholane via reductive amination / Sharaf Nawaz Khan ; Nam Ju Cho ; Hong-Seok Kim4.3:
Synthesis of Tris[(2-ethylhexanoyl)oxy]borohydride / 4.3.1:
Synthesis of 3[alpha]-Acetamino-23,24-bisnor-5[alpha]-cholane / 4.3.2:
Synthesis of 3[alpha]-N-1-[N(3-[4-Aminobutyl])-1,3-diaminopropane]-23,24-bisnor-5[alpha]-cholane / 4.3.3:
Acknowledgements
Oxidation of Primary and Secondary Alcohols / 5:
Copper(Il) catalyzed oxidation of primary alcohols to aldehydes with atmospheric oxygen / Suribabu Jammi ; Tharmalingan Punniyamurthy5.1:
Synthesis of copper(II) complex 1 / 5.1.1:
Typical procedure for the oxidation of primary alcohols to aldehydes / 5.1.2:
Solvent-free dehydrogenation of secondary alcohols in the absence of hydrogen abstractors using Robinson's catalyst / G.B.W.L Ligthart ; R.H. Meijer ; J. v. Buijtenen ; J. Meuldijk ; J.A.J.M. Vekemans ; L.A. Hulshof5.2:
Dehydrogenation of 2-Octanol using Ru(OCOCF[subscript 3])[subscript 2](CO)(PPh[subscript 3])[subscript 2] as a catalyst / 5.2.1:
2-Iodoxybenzoic acid (IBX)/n-Bu[subscript 4]NBr/CH[subscript 2]Cl[subscript 2]-H[subscript 2]O: a mild system for the selective oxidation of secondary alcohols / Krisada Kittigowittana ; Manat Pohmakotr ; Vichai Reutrakul ; Chutima Kuhakarn5.3:
Synthesis of 1-Hydroxy-5-decanone / 5.3.1:
Hydroxylation, Epoxidation and Related Reactions / 6:
Proline-catalyzed [alpha]-aminoxylation of aldehydes and ketones / Yujiro Hayashi ; Mitsuru Shoji6.1:
Synthesis of (R)-2-Anilinoxypropanol / 6.1.1:
Synthesis of (R)-7-Anilinoxy-1,4-dioxaspiro[4.5]decan-8-one / 6.1.2:
Ru/Silia Cat TEMPO-mediated oxidation of alkenes to [alpha]-hydroxyacids / Rosaria Ciriminna ; Mario Pagliaro6.2:
Synthesis of Silia Cat TEMPO / 6.2.1:
Synthesis of 2-(4-Chlorophenyl)-1,2-propanediol / 6.2.2:
Synthesis of 2-(4-Chlorophenyl)-1,2-hydroxypropanoic acid / 6.2.3:
Catalytic enantioselective epoxidation of trans-disubstituted and trisubstituted alkenes with arabinose-derived ulose / Tony K. M. Shing ; Gulice Y.C. Leung ; To Luk6.3:
Synthesis of 2[prime],3[prime]-Diisobutyl acetal / 6.3.1:
Synthesis of ulose / 6.3.2:
Asymmetric epoxidation of trans-[alpha]-Methylstilbene using ulose as catalyst at 0 [degree]C / 6.3.3:
VO(acac)[subscript 2]/TBHP catalyzed epoxidation of 2-(2-Alkenyl)phenols. highly regio- and diastereoselective oxidative cyclisation to 2,3-Dihydrobenzofuranols and 3-Chromanols / Alessandra Lattanzi ; Arrigo Scettri6.4:
VO(acac)[subscript 2]/TBHP catalyzed epoxidation of 2-(3,7-Dimethyl-octa-2,6-dienyl)-phenol / 6.4.1:
VO(acac)[subscript 2]/TBHP/TFA catalyzed oxidative cyclization of 2-(3,7-Dimethyl-octa-2,6-dienyl)-phenol / 6.4.2:
An Oxalolidinone ketone catalyst for the asymmetric epoxidation of cis-olefins / David Goeddel ; Yian Shi6.5:
Amadori rearrangement to give 1-Dibenzylamino-1-deoxy-D-fructose / 6.5.1:
Acetal protection of 1-Dibenzylamino-1-deoxy-D-fructose / 6.5.2:
Hydrogenation of the Dibenzylamine / 6.5.3:
Phosgene cyclization of aminoalcohol / 6.5.4:
Alcohol oxidation / 6.5.5:
Synthesis of ketone 2 / 6.5.6:
Asymmetric epoxidation of cis-[beta]-Methylstyrene / 6.5.7:
[alpha]-Fluorotropinone immobilised on silica: a new stereoselective heterogeneous catalyst for epoxidation of alkenes with oxone / Giovanni Sartori ; Alan Armstrong ; Raimondo Maggi ; Alessandro Mazzacani ; Raffaella Sartorio ; France Bigi ; Belen Dominguez-Fernandez6.6:
Synthesis of silica KG-60-supported enantiomerically enriched [alpha]-Fluorotropinone / 6.6.1:
Synthesis of enantiomerically enriched epoxides / 6.6.2:
Asymmetric epoxidation catalyzed by novel azacrown ether-type chiral quaternary ammonium salts under phase-transfer catalytic conditions / Kazushige Hori ; Keita Tani ; Yasuo Tohda6.7:
Synthesis of precursor of the azacrown ether / 6.7.1:
Synthesis of the azacrown ether / 6.7.2:
Synthesis of the azacrown ether-type quaternary ammonium salt / 6.7.3:
Asymmetric epoxidation of (E)-Chalcone catalyzed by the azacrown ether-type quaternary ammonium salt as chiral PTC / 6.7.4:
Enantioselective epoxidation of olefins using phase transfer conditions and a chiral [azepinium][TRISPHAT] salt as catalyst / Jerome Vachon ; Celine Perollier ; Alexandre Martinez ; Jerome Lacour6.8:
Enantioselective epoxidation of 1-Phenyl-3,4-dihydronaphthalene / 6.8.1:
Catalytic asymmetric epoxidation of [alpha],[beta]-unsaturated esters promoted by a Yttrium-biphenyldiol complex / Masakatsu Shibasaki ; Hiroyuki Kakei ; Shigeki Matsunaga6.9:
Synthesis of (aS,R)-6,6[prime]-[(Propylene)dioxy]biphenyl-2,2[prime]-diol / 6.9.1:
Synthesis of (aS,R)-2,2-[Oxybis(ethylene)dioxy]-6,6[prime]-[(propylene)dioxy]biphenyl / 6.9.2:
Synthesis of (S)-6,6[prime]-[Oxybis(ethylene)dioxy]biphenyl-2,2[prime]-diol / 6.9.3:
Enantiomeric enrichment of (S)-6,6[prime]-[Oxybis(ethylene)dioxy]biphenyl-2,2[prime]-diol / 6.9.4:
Catalytic asymmetric epoxidation of [alpha],[beta]-unsaturated esters / 6.9.5:
Catalytic enantioselective epoxidation of [alpha],[beta]-enones with a binol-zinc-complex / Ana Minatti ; Karl Heinz Dotz6.10:
Synthesis of (E)-(2S,3R)-Phenyl-(3-phenyloxiran-2-yl)methanone / 6.10.1:
Asymmetric epoxidation of Phenyl-2-(3[prime]-pyridylvinyl)sulfone using polyleucine hydrogen peroxide gel / Mike R. Pitts6.11:
Preparation of polyleucine-hydrogen peroxide gel / 6.11.1:
Synthesis of Phenyl-2-(3[prime]-pyridylvinyl) sulfone (2) / 6.11.2:
Oxidation of Ketones to Lactones or Enones / 7:
Synthesis of 2-(Phosphinophenyl)pyrindine ligand and its application to palladium-catalyzed asymmetric Baeyer-Villiger oxidation of prochiral cyclobutanones / Katsuji Ito ; Tsutomu Katsuki7.1:
Synthesis of (7R)-2-(2-Hydroxyphenyl)-7-isopropyl-6,7-dihydro-5H-1-pyrindine / 7.1.1:
2-[2-(Diphenylphosphinoyl)phenyl]-7-isopropyl-6,7-dihydro-5H-1-pyrindine / 7.1.2:
2-[2-(Diphenylphosphanyl)phenyl]-7-isopropyl-6,7-dihydro-5H-1-pyrindine / 7.1.3:
Asymmetric Baeyer-Villiger oxidation of 3-Phenylcyclobutanone / 7.1.4:
(D)-Codeinone from (D)-Dihydrocodeinone via the use of modified o-iodoxybenzoic acid (IBX). A convenient oxidation of ketones to enones / Paul Mather7.2:
Synthesis of IBX / 7.2.1:
Synthesis of codeinone / 7.2.2:
Oxidative C-C Coupling / 8:
Enantioselective oxidative coupling of 2-Naphthols catalyzed by a novel chiral vanadium complex / Nan-Sheng Xie ; Quan-Zhong Liu ; Zhi-Bin Luo ; Liu-Zhu Gong ; Ai-Qiao Mi ; Yao-Zhong Jiang8.1:
Synthesis of 3,3-Diformyl-2,2[prime]-biphenol / 8.1.1:
Synthesis of chiral vanadium complexes / 8.1.2:
Catalytic oxidative coupling of 7-Alkoxy-1-naphthols by chiral vanadium complexes / 8.1.3:
Reference
Catalytic oxidative cross-coupling reaction of 2-Naphthol derivatives / Shigeki Habaue ; Tomohisa Temma8.2:
Synthesis of Methyl 2,2[prime]-dihydroxy-1,1[prime]-binaphthalene-3-carboxylate / 8.2.1:
Oxidative coupling of benzenes with [alpha],[beta]-unsaturated aldehydes by Pd(OAc)[subscript 2]/ HPMoV/ O[subscript 2] system / Tomoyuki Yamada ; Satoshi Sakaguchi ; Yasutaka Ishii8.3:
Synthesis of Cinnamaldehyde / 8.3.1:
Oxidation of Sulfides and Sulfoxides / 9:
The first example of direct oxidation of sulfides to sulfones by an osmate-molecular oxygen system / Boyapati M. Choudary ; Chinta Reddy ; V. Reddy ; Billakanti V. Prakash ; Mannepalli L. Kantam ; B. Sreedhar9.1:
Synthesis of osmate exchanged Mg-Al layered double hydroxides (LDH-OsO[subscript 4]) / 9.1.1:
Synthesis of Methyl phenyl sulfone or Methylsulfonylbenzene / 9.1.2:
Selective oxidation of sulfides to sulfoxides and sulfones using hydrogen peroxide in the presence of zirconium tetrachloride / Kiumar Bahrami9.2:
Oxidation of Benzyl 4-bromobenzyl sulfide to Benzyl 4-bromobenzyl sulfoxide using H[subscript 2]O[subscript 2] in the presence of zirconium tetrachloride / 9.2.1:
Oxidation of Benzyl 4-bromobenzyl sulfide to Benzyl 4-bromobenzyl sulfone using H[subscript 2]O[subscript 2] in the presence of zirconium tetrachloride / 9.2.2:
WO[subscript 3]-30 % H[subscript 2]O[subscript 2]-cinchona alkaloids: a new heterogeneous catalytic system for asymmetric oxidation and kinetic resolution of racemic sulfoxides / Vinay V. Thakur ; A. Sudalai9.3:
Synthesis of (R)-2-[[[3-Methyl-4-(2,2,2-trifluoroethoxy)-2-pyridyl]methyl]sulfinyl]-1H-benzimadazole {(R)-(+)-Lansoprazole} / 9.3.1:
Synthesis of (R)-(+)-Phenyl benzyl sulfoxide / 9.3.2:
Benzyl-4,6-O-isopropylidene-[alpha]-(D)-glucopyranoside, 2-deoxy-2-[[(2-hydroxy-3,5-di-tert-butylphenyl)methylene]amino] as a ligand for vanadium-catalyzed asymmetric oxidation of sulfides / Raffaella Del Litto ; Guiseppina Roviello ; Francesco Ruffo9.4:
Synthesis of Benzyl-4,6-O-isopropylidene-[alpha]-D-glucopyranoside, 2-deoxy-2-[[(2-hydroxy-3,5-di-tert-butylphenyl)methylene]imine] / 9.4.1:
Oxidation of Thioanisole / 9.4.2:
Asymmetric sulfoxidation of aryl methyl sulfides with hydrogen peroxide in water / Alessando Scarso ; Giorgio Strukul9.5:
Synthesis of complex (R)-BINAP)PtCl[subscript 2] / 9.5.1:
Synthesis of complex [((R)-BINAP)Pt((OH)][subscript 2](BF[subscript 4])[subscript 2] / 9.5.2:
Stereoselective catalytic oxidation of aryl methyl sulfides / 9.5.3:
Index
Series Preface
Preface to Volume 5
Abbreviations
7.

図書

図書
Lutz F. Tietze, Gordon Brasche, and Kersten M. Gericke
出版情報: Weinheim : Wiley-VCH, c2006  xiv, 617 p. ; 25 cm
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Introduction
Cationic Transformations
Anionic Transformations
Radical Transformations
Transformations with Carbenes and Nitrenes
Pericyclic Transformations
Photochemical Transformations
Transition Metal Catalysed Transformations
Rearrangements
Fragmentations
Reductions
Oxidations
Introduction
Cationic Transformations
Anionic Transformations
8.

図書

図書
by Richard C. Larock
出版情報: New York : Wiley-VCH, c1999  xliii, 2583 p. ; 26 cm
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目次情報:
Quick-Start Instructions
Personalizing the COT Infobase
Searching the COT Infobase
Quick-Start Instructions
Personalizing the COT Infobase
Searching the COT Infobase
9.

図書

図書
Tse-Lok Ho
出版情報: River Edge, NJ : World Scientific, 1998  xi, 386 p. ; 23 cm
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10.

図書

図書
U.T. Bornscheuer, R.J. Kazlauskas
出版情報: Weinheim : Wiley-VCH, c1999  xiii, 336 p. ; 25 cm
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Introduction / 1:
Designing Enantioselective Reactions / 2:
Kinetic Resolutions / 2.1:
Asymmetric Syntheses / 2.2:
Choosing Reaction Media: Water and Organic Solvents / 3:
Hydrolysis in Water / 3.1:
Transesterifications and Condensations in Organic Solvents / 3.2:
Other Reaction Media / 3.3:
Immobilization / 3.4:
Protein Sources and Optimization of Biocatalyst Performance / 4:
Accessing Biodiversity / 4.1:
Creating Improved Biocatalysts / 4.2:
Catalytic Promiscuity in Hydrolases / 4.3:
Lipases and Esterases / 5:
Availability, Structures and Properties / 5.1:
Survey of Enantioselective Lipase-Catalyzed Reactions / 5.2:
Chemo-and Regioselective Lipase-Catalyzed Reactions / 5.3:
Reactions Catalyzed by Esterases / 5.4:
Proteases and Amidases / 6:
Occurrence and Availability of Proteases and Amidases / 6.1:
General Features of Subtilisin, Chymotrypsin, and Other Proteases and Amidases / 6.2:
Structures of Proteases and Amidases / 6.3:
Survey of Enantioselective Protease-and Amidase-Catalyzed Reactions / 6.4:
Phospholipases / 7:
Phospholipase A 1 / 7.1:
Phospholipase A 2 / 7.2:
Phospholipase C / 7.3:
Phospholipase D / 7.4:
Epoxide Hydrolases / 8:
Mammalian Epoxide Hydrolases / 8.1:
Microbial Epoxide Hydrolases / 8.3:
Hydrolysis of Nitriles / 9:
Mild Conditions / 9.1:
Regioselective Reactions of Dinitriles / 9.3:
Enantioselective Reactions / 9.4:
Other Hydrolases / 10:
Glycosidases / 10.1:
Haloalcohol Dehalogenases / 10.2:
Phosphotriesterases / 10.3:
Abbreviations
References
Index
Introduction / 1:
Designing Enantioselective Reactions / 2:
Kinetic Resolutions / 2.1:
11.

図書

図書
edited by André Loupy
出版情報: Weinheim : Wiley-VCH, 2002  xxiv, 499 p. ; 25 cm
シリーズ名: Green chemistry
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Volume 1
Preface
About European Cooperation in COST Chemistry Programs
List of Authors
Microwave-Material Interactions and Dielectric Properties, Key Ingredients for Mastery of Chemical Microwave Processes / Didier Stuerga)1:
Fundamentals of Microwave-Matter Interactions / 1.1:
Key Ingredients for Mastery of Chemical Microwave Processes / 1.2:
References
Development and Design of Laboratory and Pilot Scale Reactors for Microwave-assisted Chemistry / Bernd Ondruschka, Werner Bonrath, and Didier Stuerga)2:
Introduction / 2.1:
Basic Concepts for Reactions and Reactors in Organic Synthesis / 2.2:
Methods for Enhancing the Rates of Organic Reactions / 2.3:
Microwave-assisted Organic Syntheses (MAOS) / 2.4:
Commercial Microwave Reactors - Market Overview / 2.5:
Selected Equipment and Applications / 2.6:
Qualification and Validation of Reactors and Results / 2.7:
Conclusion and Future / 2.8:
Roles of Pressurized Microwave Reactors in the Development of Microwaveassisted Organic Chemistry / Thach Le Ngoc ; Brett A. Roberts ; Christopher R. Strauss)3:
Toward Dedicated Microwave Reactors / 3.1:
Applications of the New Reactors / 3.3:
Commercial Release of MBRs and CMRs / 3.4:
Advantages of Pressurized Microwave Reactors / 3.5:
Applications / 3.6:
Effect of the Properties of Microwave Heating on the Scale-up of Methods in Pressurized Reactors / 3.7:
Software Technology for Translation of Reaction Conditions / 3.8:
Conclusion. Acknowledgments / 3.9:
Nonthermal Effects of Microwaves in Organic Synthesis / Laurence Perreux and Andr?? Loupy)4:
Origin of Microwave Effects / 4.1:
Specific Nonthermal Microwave Effects / 4.3:
Effects of the Medium / 4.4:
Effects Depending on Reaction Mechanisms / 4.5:
Effects Depending on the Position of the Transition State Along the Reaction Coordinates / 4.6:
Effects on Selectivity / 4.7:
Some Illustrative Examples / 4.8:
Concerning the Absence of Microwave Effects / 4.9:
Conclusions: Suitable Conditions for Observation of Specific MW Effects / 4.10:
5 Selectivity Under the Action of Microwave Irradiation / Antonio de la Hoz ; Angel D&A?acute;az-Ortiz ; Andr??s Moreno)
Selective Heating / 5.1:
Modification of Chemoselectivity and Regioselectivity / 5.3:
Modification of Stereo and Enantioselectivity / 5.4:
Conclusions. Acknowledgments / 5.5:
Microwaves and Phase-transfer Catalysis / Andr?? Loupy ; Alain Petit ; Dariusz Bogdal)6:
Phase-transfer Catalysis / 6.1:
Synthetic Applications of Phase-transfer Processes / 6.2:
Conclusion. References / 6.3:
Microwaves and Ionic Liquids / Nicholas E. Leadbeater and Hanna M. Torenius)7:
Ionic Liquids in Conjunction with Microwave Activation / 7.1:
Use of Ionic Liquids and Microwaves in Multicomponent Reactions / 7.2.3:
Use of Ionic Liquids as Heating Aids / 7.2.4:
Conclusions / 7.3:
Abbreviations
Organic Synthesis Using Microwaves and Supported Reagents / Rajender S. Varma and Yuhong Ju)8:
Microwave-accelerated Solvent-free Organic Reactions / 8.1:
Microwave-assisted Reactions on Graphite / Thierry Besson ; ValeA'rie Thiery ; Jacques Dubac)8.3:
Graphite as a Sensitizer / 9.1:
Graphite as Sensitizer and Catalyst / 9.3:
Notes / 9.4:
Conclusion / 9.5:
Microwaves in Heterocyclic Chemistry / Jean Pierre Bazureau ; Jack Ha10:
Volume 1
Preface
About European Cooperation in COST Chemistry Programs
12.

図書

図書
editors-in-chief, Alan R. Katritzky, Otto Meth-Cohn, Charles W. Rees
出版情報: [Oxford] : Pergamon , Oxford ; New York : Elsevier Science, c1995  7 v. ; 28 cm
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13.

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図書
Jiro Tsuji
出版情報: Chichester ; New York : Wiley & Sons, 1995  xiv, 560 p. ; 24 cm
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The Basic Chemistry of Organopalladium Compounds
Classification of the Reactions Involving Pd(II) Compounds and Pd(0) Complexes in This Book
Oxidative Reactions with Pd(II) Compounds
Catalytic Reactions with Pd(0) and Pd(II)
Various Reactions Catalyzed by Pd(II) and Pd(0)
Index
The Basic Chemistry of Organopalladium Compounds
Classification of the Reactions Involving Pd(II) Compounds and Pd(0) Complexes in This Book
Oxidative Reactions with Pd(II) Compounds
14.

図書

図書
volume editor, Stanley M. Roberts
出版情報: [Oxford] : Pergamon , Oxford ; New York : Elsevier Science, c1995  xix, 1420 p. ; 28 cm
シリーズ名: Comprehensive organic functional group transformations / editors-in-chief, Alan R. Katritzky, Otto Meth-Cohn, Charles W. Rees ; v. 1
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One or more CH bond(s) by substitution: reduction of C-halogen and C-chalcogen bonds / A.G. Sutherland
One or more CH bond(s) by substitution: reduction of C-nitrogen, -phosphorus, -arsenic, -antimony, -bismuth, -carbon, -silicon, -germanium, -boron and -metal bonds / J. Howarth
Two or more CH bond(s) by addition to C-C multiple bonds / K. Jones
One or more CC bond(s) by substitution: substitution of halogen / G. Edwards
One or more CC bond(s) by substitution: substitution of chalcogen / T.N. Birkinshaw
One or more CC bond(s) by substitution: substitution of C-nitrogen -phosphorus, -arsenic, -antimony, -bismuth, -carbon, -silicon, -germanium, -boron and -metal functions / P.C.B. Page
One or more CC bond(s) by addition: addition of carbon electrophiles & nucleophiles to multiple bonds / A. Armstrong
One or more CC bond(s) by addition: addition of carbon radicals & electrocyclic additions to CC multiple bonds / A. Clark ; P. Taylor
One or more CH and/or CX bond(s) by rearrangement / I. Coldham
One or more = CH bond(s) by substitution or addition / M. Hayes
One or more =CC bond(s) by substitution or addition / P.G. Steel
One or more C=C bond(s) by addition / A.C. Regan
One or more C=C bond(s) by elimination of hydrogen, carbon, halogen, or oxygen functions / J.M. Percy
One or more C=C bond(s) by elimination of sulphur, selenium, tellurium, nitrogen, phosphorus, arsenic, antimony, bismuth, silicon, germanium, boron or metal functions / A.R. Maguire
One or more C=C Bond(s) by condensation: condensation of non-heteroatom linked functions, halides, chalcogen, or nitrogen functions / C.M. Rayner
One or more C=C bond(s) by condensation: condensation of phosphorus, arsenic, antimony, bismuth, silicon, germanium, boron or metal functions / I. Gosney ; D. Lloyd
One or more C=C bond(s) by electrocyclic processes / H. McNab
One or more =CH, =CC and/or C=C bond(s) by rearrangement / P.J. Murphy
Tricoordinate anions, cations and radicals / J.O. Williams ; M. Kelly
Allenes and cumulenes / P.H. Dixneuf ; C. Bruneau
Acetylenes / M. Furber
Ions, radicals and carbenes and of other monocoordinated systems / J. Dickinson
One or more CH bond(s) by substitution: reduction of C-halogen and C-chalcogen bonds / A.G. Sutherland
One or more CH bond(s) by substitution: reduction of C-nitrogen, -phosphorus, -arsenic, -antimony, -bismuth, -carbon, -silicon, -germanium, -boron and -metal bonds / J. Howarth
Two or more CH bond(s) by addition to C-C multiple bonds / K. Jones
15.

図書

図書
volume editor, Steven V. Ley
出版情報: [Oxford] : Pergamon , Oxford ; New York : Elsevier Science, c1995  xix, 1441 p. ; 28 cm
シリーズ名: Comprehensive organic functional group transformations / editors-in-chief, Alan R. Katritzky, Otto Meth-Cohn, Charles W. Rees ; v. 2
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Alkyl halides / P.L. Spargo
Alkyl chalcogenides: oxygen-based functional groups / J.B. Sweeney
Alkyl chalcogenides: sulphur-based functional groups / P.C.B. Page
Alkyl chalcogenides: selenium- and tellurium-based functional groups / T. Kataoka ; M. Yoshimatsu
Alkylnitrogen compounds: amines and their salts / C.M. Marson ; A.D. Hobson
Alkylnitrogen compounds: compounds with N-halogen, N-O, N-S, N-Se and N-Te functional groups / R. Bowman ; R.J. Marmon
Alkylnitrogen compounds: compounds with N-N, N-P, N-As, N-Sb, N-Bi, N-Si, N-Ge, N-B and N-metal functional groups / P.R. Huddleston ; I.G.C. Coutts
Alkylphosphorus compounds / J.C. Tebby ; D. Genov ; J.W. Wheeler
Alkyl arsenic, -antimony and -bismuth compounds (Mei-Xiang Wang
Alkyl -silicon, -germanium and -boron compounds / E.W. Colvin ; M. Wills
Alkylmetals / S.V. Ley ; C. Kouklovsky
Vinyl and aryl halides / C.J. Urch
Vinyl and aryl chalcogenides: oxygen-based functional groups / C.K-F. Chiu
Vinyl and aryl chalcogenides: sulphur-, selenium- and tellurium-based functional groups / P. Taylor
Vinyl- and aryl-nitrogen compounds / G. SauvT ; V. Rao
Vinyl- and aryl phosphorus derivatives / T. Minami
Vinyl- and aryl arsenic, -antimony and -bismuth functions / R.W. Read
Vinyl- and aryl-silicon, -germanium and boron compounds / L. Hevesi
Vinyl- and aryl-metals / E. Negishi
Stabilized substituted ions and radicals bearing one heteroatom / S.D. Lindell
Alkynyl halides and chalcogenides / P.J. Stang ; V.V. Zhdankin
Alkynyl nitrogen and -phosphorus compounds / K.I. Booker-Milburn
Alkynyl-arsenic, -antimony, -bismuth, -silicon, -germanium -boron and -metal compounds / W. Kitching ; K. Kwetkat
Alkyl halides / P.L. Spargo
Alkyl chalcogenides: oxygen-based functional groups / J.B. Sweeney
Alkyl chalcogenides: sulphur-based functional groups / P.C.B. Page
16.

図書

図書
volume editor, Gerald Pattenden
出版情報: [Oxford] : Pergamon , Oxford ; New York : Elsevier Science, c1995  xix, 941 p. ; 28 cm
シリーズ名: Comprehensive organic functional group transformations / editors-in-chief, Alan R. Katritzky, Otto Meth-Cohn, Charles W. Rees ; v. 3
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Aldehydes: alkyl aldehydes / K.E.B. Parkes ; S. Richardson
agr; bgr;-unsaturated aldehydes / W. Ebenezer ; P. Wight
Aryl and heteroaryl aldehydes / D.G. Hollingworth ; D. Walter
Ketones: dialkyl ketones / K.E. Parkes
agr; bgr;-unsaturated ketones
Ketones bearing an agr;, bgr;-aryl or -heteroaryl substituent
O-substituted aldehydes and ketones / D.A. Whiting
Thioaldehydes and thioketones / W. Whittingham
Selenio- and tellurio-aldehydes and ketones / F.S. Guziec ; L. Guziec
Imines and their N-substituted derivatives: NH, NR and N- haloimines / G.M. Robertson
Imines and their N-substituted derivatives: oximes and their S, Se and Te analogues / R.C.F. Jones
Imines and their N-substituted derivatives: hydrazones and other =NN derivatives including diazo- compounds / J.S. Clark
P, As, Sb, and Bi ylides / D. Gilheany, Eacute;. Coyne
Doubly bonded metalloid functions / Si, Ge, B. M.A. McKervey ; Tao Ye
Doubly bonded metal functions / M.A. McKervey
Ketenes, their cumulene analogues and their S, Se and Te analogues / D. Harrowven
Ketenimines and their P, As, Sb and Bi analogues / J.P. Michael ; C.B. De Koning
Nitriles: general methods and aliphatic nitriles / M. North
Nitriles: agr; bgr;-unsaturated and aryl nitriles / M.J. Kiefel
N-substituted nitriles and other heteroanalogues of nitriles of the type RCZ / R.M. Paton
Isocyanides and their heteroanalogues (RZC) / I.A. O'Neil
Aldehydes: alkyl aldehydes / K.E.B. Parkes ; S. Richardson
agr; bgr;-unsaturated aldehydes / W. Ebenezer ; P. Wight
Aryl and heteroaryl aldehydes / D.G. Hollingworth ; D. Walter
17.

図書

図書
volume editor, Gordon W. Kirby
出版情報: [Oxford] : Pergamon , Oxford ; New York : Elsevier Science, c1995  xix, 1352 p. ; 28 cm
シリーズ名: Comprehensive organic functional group transformations / editors-in-chief, Alan R. Katritzky, Otto Meth-Cohn, Charles W. Rees ; v. 4
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Dihaloalkanes / R.A. Hill
Functions incorporating a halogen and a chalcogen / N.W.A. Geraghty
Functions incorporating a halogen and another heteroatom group other than a chalcogen / A.C. Campbell ; D. Jaap
Functions bearing two oxygens / H.K. Rami ; D.T. MacPherson
Functions incorporating oxygen and another chalcogen / R.H. Wightman
Functions incorporating two chalcogens other than oxygen / Y. Valleacute;e ; A. Bulpin
Functions incorporating a chalcogen and a group V element / J.D. Hepworth ; C. Gabbutt
Functions incorporating a chalcogen and a silicon, germanium, boron or metal / M. Gough ; J. Steele
Functions bearing two nitrogens / D.R. Buckle ; I.L. Pinto
Functions incorporating a nitrogen and another group V element / M. Heaney
Functions incorporating a nitrogen and a silicon, germanium, boron or metal
Functions containing one phosphorus and either another phosphorus or As, Sb, Bi, Si, Ge, B or a metal / R.A. Aitken
Functions containing at least one As, Sb or Bi together with a metalloid (Si, Ge or B) or a metal / W.M. Horspool
Functions containing at least one metalloid (Si, Ge or B) together with another metalloid or metal / C. Barber
Functions containing two atoms of the same metallic element / W.J. Kerr ; P.L. Pauson
Functions containing two different atoms of metallic elements
Functions incorporating two halogens or a halogen and a chalcogen / R. Westwood ; N. Westwood ; P.D. Kennewell
Functions incorporating a halogen and another group other than a halogen or a chalcogen / D.I. Smith
Functions bearing two chalcogens / G.N. Sheldrake
Functions containing a chalcogen and any other group than a halogen or a chalcogen
Functions containing at least one nitrogen and no halogen or chalcogen / G.L. Patrick
Functions containing at least one phosphorus, arsenic, antimony or bismuth and no halogen, chalcogen or nitrogen / J. Berge
Functions containing at least one metalloid (Si, Ge or B) and no halogen, chalcogen or group V element; also of functions containing two metals / R.A.B. Webster
Tri- and di-coordinated ions, radicals and carbenes bearing two heteroatoms
Dihaloalkanes / R.A. Hill
Functions incorporating a halogen and a chalcogen / N.W.A. Geraghty
Functions incorporating a halogen and another heteroatom group other than a chalcogen / A.C. Campbell ; D. Jaap
18.

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図書
volume editor, Christopher J. Moody
出版情報: [Oxford] : Pergamon , Oxford ; New York : Elsevier Science, c1995  xix, 1442 p. ; 28 cm
シリーズ名: Comprehensive organic functional group transformations / editors-in-chief, Alan R. Katritzky, Otto Meth-Cohn, Charles W. Rees ; v. 5
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Acyl halides / J. Williams
Carboxylic acids / M.A. Ogliaruso ; J.F. Wolfe
Carboxylic esters / J. Mulzer
Other acyloxy compounds / P.T. Gallagher ; J. Gilmore
Acyl-sulphur, -selenium or -tellurium functions / A.Ogawa
Amides / P.D. Bailey ; I.D. Collier ; K.M. Morgan
N-hetero- substituted amides / R.D. Connell
Acylphosphorus, -arsenic, -antimony or -bismuth functions / K. Afarinkia ; M.V. Vinader
Acyl-silicon, -germanium or -boron functions / D.P. Curran ; H. Qi
Acyl metal functions / P. Warner
Thio-, seleno- and tellurio-acyl halides / A. Williams
Thio-, seleno- and tellurio- acyloxy functions / J. Nakayama ; A. Ishii
Functions with two chalcogens other than oxygen / S. Kato ; T. Murai
Thionoamides and their Se and Te analogues / C.P.Dell
N-hetero-substituted thionoamides and their Se and Te analogues / M. Owton
Thioacyl functions linked to a metalloid (Si, Ge or B) or metal; and their selenio and tellurio analogues / A.D. Jones
Iminoacyl halides and oxy functions / W. Kantlehner ; W.W. Mergen
Iminoacyl functions linked to other chalcogens / S. Challenger
Amidines and N-substituted amidines / P.J. Dunn
Iminoacyl functions linked to any other heteroatom / M. Butters
N-hetero-substituted iminoacyl functions / B. Stanovnik
Diazomethanes linked to atoms other than carbon
Phosphoacyl functions and their As, Sb and Bi analogues / L. Weber
Functions doubly bonded to Si, Ge or B / B.P. Clark
Functions doubly bonded to a metal / P. Quayle
Functions with at least one oxygen (Y=C=O) / P. Molina ; A. Tarraga
Functions with at least one chalcogen other than oxygen
Functions with at least one nitrogen and no chalcogens / R. Muthyala
Functions with heteroatoms other than chalcogen or nitrogen
Nitriles with a heteroatom attached to the cyano-carbon / I.K. Boddy ; M.J. Ford
Other triply-bonded heteroatom derivatives / M. Regitz
Acyl halides / J. Williams
Carboxylic acids / M.A. Ogliaruso ; J.F. Wolfe
Carboxylic esters / J. Mulzer
19.

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図書
volume editor, Thomas L. Gilchrist
出版情報: [Oxford] : Pergamon , Oxford ; New York : Elsevier Science, c1995  xix, 933 p. ; 28 cm
シリーズ名: Comprehensive organic functional group transformations / editors-in-chief, Alan R. Katritzky, Otto Meth-Cohn, Charles W. Rees ; v. 6
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Trihalides / R.D. Chambers ; J. Hutchinson
Functions containing halogens and any other elements / G.B. Jones
Functions containing three chalcogens (and no halogens) / G. Mitchell
Functions containing a chalcogen and any other heteroatoms other than a halogen / M.J. Rice
Functions containing at least one group V element (and no halogen or chalcogen) / D.P.J. Pearson
Functions containing at least one metalloid (Si, Ge, or B) and no halogen, chalogen or group V element; also functions containing three metals / V. Ramanenko
Functions containing four halogens, or three halogens and one other heteroatom substituent / A. Senning ; A.H. Gouliaev
Functions containing two halogens and two other heteroatom substituents / A. Varvoglis
Functions containing one halogen and three other heteroatom substituents / P. Savignac ; A. Marinetti
Functions containing four or three chalcogens and no halogens
Functions containing two or one chalcogen (and no halogens) / W. Petz ; F. Weller
Functions containing at least one group V element (and no halogen or chalcogen) (Ph
Savignac / D. Carmichal
Functions containing at least one metalloid (Si,Ge or B) and no halogen, chalcogen or group V element; also functions containing four metals / P.D. Lickiss
Functions containing a carbonyl group and at least one halogen / G.E. Gymer ; S. Narayanaswami
Functions containing a carbonyl group and at least One chalcogen (but no halogen) / H. Eckert
Functions containing a carbonyl group and two heteroatoms other than a halogen or chalcogen / A.F. Hegarty
Functions containing a thiocarbonyl group and at least Oone halogen; also at least one chalcogen and no halogen / K. Pihlaja ; E. Kleinpeter
Functions containing a thiocarbonyl group bearing two heteroatoms other than a halogen or chalcogen / J. Barluenga
Functions containing a selenocarbonyl or tellurocarbonyl group / F.S. Guziec Jr ; L.J. Guziec
Functions containing an iminocarbonyl group and at least one halogen; also one chalcogen and no halogen / T.L. Gilchrist
Functions containing an iminocarbonyl group and any elements other than a halogen or chalcogen / I.A. Cliffe
Functions containing doubly bonded P, As, Sb, Bi, Ge, B or a metal / V.D. Romanenko ; M. Sanchez ; L. Lamande
Tricoordinated stabilized cations and radicals, + CXYZ and bull; CXYZ
Trihalides / R.D. Chambers ; J. Hutchinson
Functions containing halogens and any other elements / G.B. Jones
Functions containing three chalcogens (and no halogens) / G. Mitchell
20.

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図書
Tse-Lok Ho
出版情報: New York : Wiley, c1994  xi, 450 p. ; 25 cm
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Convergency and Reiterative Processes
Activity Modulation, Group Protection, and Latent Functionalities
Umpolung
Tandem Reactions
Cyclic Arrays for Structural and Stereochemical Manipulations
Intramolecularization and Neighboring Group Participations
Template and Chelation Effects
Symmetry Considerations
Miscellaneous Tactics
References
Index
Convergency and Reiterative Processes
Activity Modulation, Group Protection, and Latent Functionalities
Umpolung
21.

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図書
Zorbach, W. Werner ; Tipson, R. Stuart
出版情報: New York : Interscience Publishers, c1973  x, 674 p. ; 23 cm
シリーズ名: An Interscience series ; . Synthetic procedures in nucleic acid chemistry / edited by W. Werner Zorbach and R. Stuart Tipson <BA11068644> v. 2
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22.

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図書
by C. W. Bird
出版情報: London : Logos P. , New York ; London : Academic P, [1967]  vii, 280 p. ; 23 cm
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23.

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図書
editor-in-chief, P.H. Groggins
出版情報: New York : McGraw-Hill, 1958  x, 1070 p. ; 24 cm
シリーズ名: McGraw-Hill chemical engineering series
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24.

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図書
W. P. Weber, G. W. Gokel
出版情報: Berlin ; New York : Springer-Verlag, 1977  xv, 280 p. ; 25 cm
シリーズ名: Reactivity and structure : concepts in organic chemistry ; v. 4
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25.

図書

図書
J. Mulzer ... [et al.]
出版情報: Weinheim ; New York : VCH, c1991-  v. ; 25 cm
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Preface
List of Contributors
Synthetic Methods / Part I.:
Direct Conversion of Sugar Glycosides into Carbocycles / Peter I. Dalko ; Pierre Sinay
Synthesis of Diaryl Ethers: A Long-Standing Problem Has Been Solved / Fritz Theil
Take The Right Catalyst: Palladium-Catalyzed CC-, CN- and CO-Bond Formation on Chloro-Arenes / Rainer Sturmer
Alkyne Metathesis in Natural Product Synthesis / Thomas Lindel
Transition Metal-Catalyzed Functionalization of Alkanes / Oliver Seitz
An Eldorado for Homogeneous Catalysis? / Gerald Dyker
New and Selective Transition Metal Catalyzed Reactions of Allenes / A. Stephen K. Hashmi
Controlling Stereoselectivity with the Aid of a Reagent-Directing Group / Bernhard Breit
Solvent-Free Organic Syntheses / Jurgen O. Metzger
Fluorous Techniques: Progress in Reaction-Processing and Purification / Ulf Diederichsen
Recent Developments in Using Ionic Liquids as Solvents and Catalysts for Organic Synthesis / Peter Wasserscheid
Recent Advances on the Sharpless Asymmetric Aminohydroxylation / Dmitry Nilov ; Oliver Reiser
Asymmetric Phase Transfer Catalysis / Christabel Carter ; Adam Nelson
Asymmetric Catalytic Aminoalkylations: New Powerful Methods for the Enantioselective Synthesis of Amino Acid Derivatives, Mannich Bases, and Homoallylic Amines / Michael Arend ; Xiaojing Wang
IBX--New Reactions with an Old Reagent / Thomas Wirth
Parallel Kinetic Resolutions / Jason Eames
The Asymmetric Baylis-Hillman-Reaction / Peter Langer
Simple Amino Acids and Short-Chain Peptides as Efficient Metal-free Catalysts in Asymmetric Synthesis / Harald Groger ; Jorg Wilken ; Albrecht Berkessel
Recent Developments in Catalytic Asymmetric Strecker-Type Reactions / Larry Yet
Highly Enantioselective or Not?--Chiral Monodentate Monophosphorus Ligands in the Asymmetric Hydrogenation / Igor V. Komarov ; Armin Borner
Improving Enantioselective Fluorination Reactions: Chiral N-Fluoro Ammonium Salts and Transition Metal Catalysts / Kilian Muniz
Catalytic Asymmetric Olefin Metathesis / Amir H. Hoveyda ; Richard R. Schrock
Activating Protecting Groups for the Solid Phase Synthesis and Modification of Peptides, Oligonucleotides and Oligosaccharides
Traceless Linkers for Solid-Phase Organic Synthesis / Florencio Zaragoza Dorwald
Merging Solid-Phase and Solution-Phase Synthesis: The "Resin-Capture-Release" Hybrid Technique / Andreas Kirschning ; Rudiger Wittenberg
Polymeric Scavenger Reagents in Organic Synthesis / Michael Watkinson
Applications / Part II.:
Total Syntheses of Vancomycin / Lars H. Thoresen ; Kevin Burgess
Bryostatin and Their Analogues
Eleutherobin: synthesis, Structure/Activity Relationship, and Pharmacophore
Total Synthesis of the Natural Products CP-263,114 and CP-225,917 / Katrin B. Lorenz
Polyene Cyclization to Adociasulfate 1 / Cordula Hopmann
Sanglifehrin A: An Immunosuppressant Natural Product from Malawi
Short Syntheses of the Spirotryprostatins
The Chemical Total Synthesis of Proteins
Solid-Phase Synthesis of Oligosaccharides / Thomas Wagner
Polymer-Supported Synthesis of Non-Oligomeric Natural Products / Stefan Sommer ; Rolf Breinbauer ; Herbert Waldmann
Explosions as a Synthetic Tool? Cycloalkynes as Precursors to Fullerenes, Buckytubes and Buckyonions / Rudiger Faust
Dendralenes: From a Neglected Class of Polyenes to Versatile Starting Materials in Organic Synthesis / Henning Hopf
Fascinating Natural and Artificial Cyclopropane Architectures
Index
New Methods and Reagents for Organic Synthesis
Carbohydrate Complexes in Enantioselective Carbon-Carbon Bond Formation
Iron eta5-Complexes in Organic Synthesis
Enzymatic Synthesis of O-Glycosides
Polycyclization as a Strategy in the Synthesis of Complex Alkaloids
Hypervalent Iodine Reagents
CC-1065: One of the Most Powerful Anti-Tumor Compounds
Total Synthesis of Rapamycin
New Methods in Stereoselective Synthesis Transition Metal/Organometallic Methods Enantioselective Catalysis / Part I:
Total Synthesis of Natural Products Synthesis of Non-Natural Compounds and Materials Solid-Phase Synthesis and Combinatorial Methods / Part II:
Preface
List of Contributors
Synthetic Methods / Part I.:
26.

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図書
[by] George R. Pettit
出版情報: New York : Van Nostrand Reinhold Co, [1972-  v ; 24 cm
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27.

図書

図書
[by] Romeo B. Wagner [and] Harry D. Zook
出版情報: New York : Wiley, 1953  xii, 887 p. ; 22 cm
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28.

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図書
by Jürgen Falbe ; translated by Charles R. Adams
出版情報: Berlin ; New York : Springer-Verlag, 1970  ix, 219 p. ; 24 cm
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29.

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図書
Gary E. Means, Robert E. Feeney
出版情報: San Francisco : Holden-Day, c1971  x, 254 p. ; 23 cm
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30.

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図書
edited by R. Daniel Little and Norman L. Weinberg
出版情報: New York : M. Dekker, c1991  xxxiii, 434 p. ; 24 cm
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31.

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図書
editor, K. Smith
出版情報: New York : Ellis Horwood : PTR Prentice Hall, 1992  xiv, 338 p. ; ill. : 24 cm
シリーズ名: Ellis Horwood PTR Prentice Hall organic chemistry series
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32.

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図書
Eckehard V. Dehmlow ... [et al.]
出版情報: Weinheim : Verlag Chemie, c1975-1979  6 v. ; 20 cm
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33.

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図書
edited by Leroy B. Townsend, R. Stuart Tipson
出版情報: New York : John Wiley, c1978-[c1991]  4 v. ; 24 cm
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34.

図書

図書
W. Carruthers
出版情報: Oxford, England ; New York : Pergamon Press, 1990  viii, 373 p. ; 25 cm
シリーズ名: Tetrahedron organic chemistry series ; v. 8
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目次情報: 続きを見る
Section headings and selected subheadings: The Diels-Alder Reaction - General Aspects.lt;/b> The dienophile
Hetero-dienophiles - aldehydes, thiocarbonyl compounds, N-sulphinylsulphonamides, imines, nitroso compounds
The diene
ortholt;/i>-Quinodimethanes
Heterodienes
Reactions in water
Reactions under high pressure
Catalysis by Lewis acids
Regiochemistry
Stereochemistry
Asymmetric reactions
Retro reactions
Intermolecular Diels-Alder Reactions.lt;/b> Stereoselectivity
Hetero-substituted dienes and dienophiles
with alkoxy- and silyloxy-dienes
alphabeta-Unsaturated aldehydes as dienes
Imines as dienophiles
Nitroso compounds as dienophiles-synthesis of 4-amino-alcohols
N-Sulphinylsulphonamides-synthesis of vicinal amino-alcohols
Synthesis of benzene derivatives
Synthesis of quinones
Intramolecular Diels-Alder Reactions.lt;/b> Stereoselectivity
Diastereoselection
Synthesis of terpenoids
Synthesis of alkaloids
Nitroso compounds
Miscellaneous [4+2] Cycloadditions.lt;/b> Allyl anions and allyl cations
Oxyallyl cations
Pentadienyl cations
Cycloadditions with trimethylenemethane
metalt;/i>-Photocycloaddition to benzene derivatives
Cobalt-catalysed trimerisation of acetylenes
[4+4] cycloaddition of 1,3-dienes
The Ene Reaction.lt;/b> Hetero-ene reactions
Intramolecular ene reactions
Magnesio-ene reaction
1,3-Dipolar Cycloaddition Reactions.lt;/b> Stereoselectivity
Azomethine ylides
Nitrile oxides
Azides, azomethine imines and diazoalkanes
[2+2] Cycloaddition Reactions.lt;/b> Ketenes
Ketene-imminium salts
Photocycloaddition to enones
De Mayo reaction
Copper-catalysed photocycloaddition of hepta-1,6-dienols
Paterno-Buchi reaction
Index
Section headings and selected subheadings: The Diels-Alder Reaction - General Aspects.lt;/b> The dienophile
Hetero-dienophiles - aldehydes, thiocarbonyl compounds, N-sulphinylsulphonamides, imines, nitroso compounds
The diene
35.

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図書
W. A. Smit, A. F. Bochkov, R. Caple
出版情報: Cambridge : Royal Society of Chemistry, c1998  xix, 477 p. ; 24 cm
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Goals of an Organic Synthesis
Tactics of Synthesis
Strategy of Synthesis
Molecular Design
Instead of Conclusion
Subject Index
Goals of an Organic Synthesis
Tactics of Synthesis
Strategy of Synthesis
36.

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図書
Timothy C. Parker and Seth R. Marder
出版情報: Cambridge : Royal Society of Chemistry, c2015  xii, 284 p. ; 24 cm
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37.

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図書
edited by Hisashi Yamamoto and Kazuaki Ishihara
出版情報: Weinheim : Wiley-VCH, c2008  2 v. ; 25 cm
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Introduction and Combined Acid Catalysis Super Bronsted Acids Chiral
Bronsted Acids Li(I), Na(I) and K(I) Lewis Acids Mg(II), CA(II) and Zn(II) Lewis Acids B(III)
Lewis Acids Al(III) Lewis Acids Ga(III) Lewis Acids In(III) Lewis Acids Si(IV)
Lewis Acids Sn(II) and Sn(IV) Lewis Acids Bi(III) Lewis Acids Sc(III) and Y(III)
Lewis Acids Lanthanide Lewis Acids Ti(IV) Lewis Acids Zr(IV) and Hf(IV)
Lewis Acids Transition Metal Lewis Acids: From Vanadium to Platinum Cu(I) and Cu(II)
Lewis Acids Ag(I) and Au(I) Lewis Acids Polymer-Supported Metal Lewis Acids
Introduction and Combined Acid Catalysis Super Bronsted Acids Chiral
Bronsted Acids Li(I), Na(I) and K(I) Lewis Acids Mg(II), CA(II) and Zn(II) Lewis Acids B(III)
Lewis Acids Al(III) Lewis Acids Ga(III) Lewis Acids In(III) Lewis Acids Si(IV)
38.

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図書
Peter G.M. Wuts and Theodora W. Greene
出版情報: Hoboken, N.J. : John Wiley & Sons, c2007  xxviii, 1082 p. ; 25 cm
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Preface to the Fourth Edition
Preface to the Third Edition
Preface to the Second Edition
Preface to the First Edition
Abbreviations
The Role of Protective Groups in Organic Synthesis / 1:
Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols / 2:
Ethers
Esters
Protection for 1,2- and 1,3-Diols
Protection for Phenols and Catechols / 3:
Protection for Phenols
Silyl Ethers
Carbonates
Aryl Carbamates
Phosphinates
Sulfonates
Protection for Catechols
Cyclic Acetals and Ketals
Cyclic Esters
Protection for 2-Hydroxybenzenethiols
Protection for the Carbonyl Group / 4:
Acetals and Ketals
Miscellaneous Derivatives
Monoprotection of Dicarbonyl Compounds
Protection for the Carboxyl Group / 5:
Amides and Hydrazides
Protection of Boronic Acids
Protection of Sulfonic Acids
Protection for the Thiol Group / 6:
Thioethers
Thioesters
Protection for the Amino Group / 7:
Carbamates
Amides
Special -NH Protective Groups
Protection for Imidazoles, Pyrroles, Indoles, and other Aromatic Heterocycles
Protection for the Amide -NH
Protection for the Sulfonamide -NH
Protection for the Alkyne -CH / 8:
Protection for the Phosphate Group / 9:
Some General Methods for Phosphate Ester Formation
Removal of Protective Groups from Phosphorus
Alkyl Phosphates
Phosphates Cleaved by Cyclodeesterifi cation
Benzyl Phosphates
Phenyl Phosphates
Photochemically Cleaved Phosphate Protective Groups
Amidates
Reactivities, Reagents, and Reactivity Charts / 10:
Reactivities
Reagents
Reactivity Charts
Protection for the Hydroxyl Group: Ethers
Protection for the Hydroxyl Group: Esters
Protection for the Amino Group: Carbamates
Special-NH Protective Groups
Protection for the Amino Group: Amides
Protection for the Amino Group: Special -NH Protective Groups
Selective Deprotection of Silyl Ethers / 11:
Index
Protection for the Alkyne-CH
Phosphates Cleaved by Cyclodeesterification
Protection for 1,2-and 1,3-Diols
Preface to the Fourth Edition
Preface to the Third Edition
Preface to the Second Edition
39.

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図書
C.H. Wong and G.M. Whitesides
出版情報: Oxford ; New York : Pergamon, 1994  xvii, 370 p. ; 26 cm
シリーズ名: Tetrahedron organic chemistry series ; v. 12
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Preface
Acknowledgements
General Aspects
Rate acceleration in enzyme-catalyzed reactions
Michaelis-Menten kinetics
Enzyme inhibition
Specificity
Improvement or alteration of enzyme specifity
Enzyme stabilization and reactor configuration
Cofactor regeneration
Enzyme catalysis in organic solvents
Multienzyme systems and metabolic engineering
Rational design of new enzymatic catalysts
Conclusion
References
Use of Hydrolytic Enzymes: Amidases, Proteases, Esterases, Lipases, Nitrilases, Phosphatases, Epoxide Hydrolases
Amidases
Protease-catalyzed peptide synthesis
Proteases that act as esterases
Acetylcholine esterase
Pig liver esterase
Phospholipases
Cholesterol esterase
Lipases
Nitrile hydrolysis enzymes
Epoxide hydrolase
Phosphatase
Oxidoreductions
Nicotinamide cofactor dependent oxidoreductions
Dehydrogenases which utilize ketoacids as substrates
Other NAD(P)-dependent dehydrogenases
Oxidoreductases that are metalloenzymes
C-C Bond Formation
Aldol condensation
Ketol and aldol transfer reaction
Addition of HCN to aldehydes
Acyloin condensation
C-C bond forming reactions involving acetyl co
Isoprenoid and steroid synthesis. bgr;-replacement of chloroalanine / A:
C-C bond formation catalyzed by vitamin B 12
Synthesis of Glycoside Bonds
Background
Glycosyltransferases of the Leloir pathway
Substrate specificity and synthetic applications of glycosyltransferases
Non-Leloir glycosyltransferases
Glycosidases
Transglycosidases
Synthesis of N-glycosides
Biological applications of synthetic glycoconjugates
Future opportunities
Addition, Elimination and Other Group Transfer Reactions (Phosphoryl-, Methyl-, Sulpho- and Amino-Transfer Reactions)
Addition of water to alkenes: fumarase
Addition of ammonia to double bonds: ammonia lyases
Transamination: aminotransferases
Addition and elimination of carboxyl group
Nucleoside triphosphate requiring enzymatic reactions
Preparation of ATP chiral at agr;-, bgr;- or ggr;-phosphorous
Phosphorothioate-containing DNA and RNA. DNA and RNA oligomers
Incorporation of modified or unnatural bases into DNA or RNA
Dehalogenation
Synthesis of chiral methyl groups
S-Adenosylmethionine and transmethylation
Sulfate activation and transfer reactions
Subject index
Preface
Acknowledgements
General Aspects
40.

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図書
Theodora W. Greene and Peter G.M. Wuts
出版情報: New York : Wiley, c1991  xvi, 473 p. ; 25 cm
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The Role of Protective Groups in Organic Synthesis
Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols
Protection for Phenols and Catechols
Protection for the Carbonyl Group
Protection for the Carboxyl Group
Protection for the Thiol Group
Protection for the Amino Group
Protection for the Alkyne-CH
Protection for the Phosphate Group
Reactivities, Reagents, and Reactivity Charts
Index
The Role of Protective Groups in Organic Synthesis
Protection for the Hydroxyl Group, Including 1,2- and 1,3-Diols
Protection for Phenols and Catechols
41.

図書

図書
Rolf Carlson
出版情報: Amsterdam ; New York : Elsevier, 1992  xvi, 536 p. ; 26 cm
シリーズ名: Data handling in science and technology ; v. 8
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42.

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図書
[edited by] Matthias Beller, Carsten Bolm
出版情報: Weinheim ; Chichester : Wiley-VCH, c1998  2 v. ; 25 cm
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目次情報: 続きを見る
Preface.
General. / 1:
Basic Aspects of Organic Synthesis with Transition Metals (Barry M. Trost). / 1.1:
Concepts for the Use of Transition Metals in Industrial Fine Chemical Synthesis (Wilhelm Keim). / 1.2:
Transition Metal-Catalyzed Reactions. / 2:
Hydroformylation: Applications in the Synthesis of Pharmaceuticals and Fine Chemicals (Matthias Beller and Kamal Kumar). / 2.1:
New Synthetic Applications of Tandem Reactions under Hydroformylation Conditions (Peter Eilbracht and Axel M. Schmidt). / 2.2:
Multiple Carbon-Carbon Bond Formations under Hydroformylation Conditions (Peter Eilbracht and Axel M. Schmidt). / 2.3:
Hydrocarboxylation and Hydroesterification Reactions Catalyzed by Transition Metal Complexes (Bassam El Ali and Howard Alper). / 2.4:
The Amidocarbonylation of Aldehydes (Axel Jacobi von Wangelin, Helfried Neumann, Dirk Gordes, and Matthias Beller). / 2.5:
Transition Metal-catalyzed Alkene and Alkyne Hydrocyanations (Albert L. Casalnuovo and T.V. Rajan Babu). / 2.6:
Cyclopropanation (Andreas Pfaltz). / 2.7:
Cyclomerization of Alkynes (H. Bonnemann and W. Brijoux). / 2.8:
Coupling of Aryl and Alkyl Halides with Organoboron Reagents (Suzuki Reaction) (Alexander Zapf). / 2.9 Isomerization of Olefin and the Related Reactions (Sei Otsuka and Kazuhide Tani).:
Transition Metal-Catalyzed Arylation of Amines and Alcohols (Alexander Zapf, Matthias Beller, and Thomas H. Riermeier). / 2.11:
Catalytic Enantioselective Alkylation of Alkenes by Chiral Metallocenes (Amir H. Hoveyda). / 2.12:
Palladium-Catalyzed Olefinations of Aryl Halides (Heck Reaction) and Related Transformations (Matthias Beller, Alexander Zapf, and Thomas H. Riermeier). / 2.13:
Palladium-Catalyzed Allylic Substitutions (Andreas Heumann). / 2.14:
Alkene and Alkyne Metathesis in Organic Synthesis (Oliver R. Thiel). / 2.15:
Homometallic Lanthanoids in Synthesis: Lanthanide Triflate-catalyzed Synthetic Reactions (Sh&umarc; Kobayashi). / 2.16:
Lanthanide Complexes in Asymmetric Two-Center Catalysis (Masakatsu Shibasaki, Hiroaki Sasai, and Naoki Yoshikawa). / 2.17:
Bismuth Reagents and Catalysts in Organic Synthesis (Axel Jacobi von Wangelin). / 2.18:
Transition Metal-Mediated Reactions. / 3:
Fischer-Type Carbene Complexes (Karl Heinz Dotz and Ana Minatti). / 3.1:
Titanium-Carbene Mediated Reactions (Nicos A. Petasis). / 3.2:
The McMurry Reaction and Related Transformations (Alois Furstner). / 3.3:
Chromium(II)-Mediated and -Catalyzed C-C Coupling Reactions (David M. Hodgson and Paul J. Comina). / 3.4:
Manganese(III)-Based Oxidative Free-Radical Cyclizations (Barry B. Snider). / 3.5:
Titanium-Mediated Reactions (Rudolf O. Duthaler, Frank Bienewald, and Andreas Hafner). / 3.6:
Zinc-Mediated Reactions (Axel Jacobi von Wangelin and Mathias U. Frederiksen). / 3.7:
The Conjugate Addition Reaction (A. Alexakis). / 3.8:
Carbometalation Reactions of Zinc Enolate Derivatives (Daniella Banon-Tenne and Ilan Marek). / 3.9:
Iron Acyl Complexes (Karola Ruck-Braun). / 3.10:
Iron-Diene Complexes (Hans-Joachim Knolker). / 3.11:
Chromium-Arene Complexes (Hans-Gunther Schmalz and Florian Dehmel). / 3.12:
Pauson-Khand Reactions (D. Strubing and M. Beller). / 3.13:
Subject Index.
Preface.
General. / 1:
Basic Aspects of Organic Synthesis with Transition Metals (Barry M. Trost). / 1.1:
43.

図書

図書
edited by Norbert Krause and Stephen Hashmi
出版情報: Weinheim : Wiley-VCH, c2004  2 v. (xv, 592 ; xi, 1143 p.) ; 25 cm
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目次情報: 続きを見る
I Synthesis of Allenes. / Volume 1:
Synthesis of Allenes by Isomerization Reactions / A. Stephen ; K. Hashmi.1:
Introduction. / 1.1:
Prototropic Rearrangements and Related Reactions of Alkynes. / 1.2:
Sigmatropic Rearrangements. / 1.3:
Rearrangements of Other Systems with at Least Two p-Bonds. / 1.4:
Retro-Ene Reactions. / 1.5:
Electrocyclic Ring Openings. / 1.6:
Intramolecular Conjugate Additions. / 1.7:
Complex Reactions and Rearrangements. / 1.8:
Conclusion. / 1.9:
Metal-Mediated Synthesis of Allenes / Anja Hoffmann-R&oder ; Norbert Krause.2:
Copper-Mediated Synthesis of Allenes. / 2.1:
Lithium-, Magnesium- and Zinc-Mediated Synthesis of Allenes. / 2.3:
Aluminum- and Indium-Mediated Synthesis of Allenes. / 2.4:
Titanium- and Samarium-Mediated Synthesis of Allenes. / 2.5:
Transition Metal-Catalyzed Synthesis of Allenes / Masamichi Ogasawara ; Tamio Hayashi.2.6:
Formation of Allenes by Substitution Reactions. / 3.1:
Formation of Allenes by Addition Reactions. / 3.3:
Formation of Allenes by Elimination Reactions. / 3.4:
Other Miscellaneous Methods of Preparing Allenes. / 3.5:
Formation of 1,2,3-Butatrienes. / 3.6:
Enantioselective Synthesis of Allenes / Hiroaki Ohno ; Yasuo Nagaoka ; Kiyoshi Tomioka.3.7:
Chirality Transfer from Propargylic Compounds. / 4.1:
Elimination Reactions of Chiral Allylic Compounds. / 4.3:
Synthesis of Allenes Using Chiral Reagents. / 4.4:
Direct Asymmetric Synthesis of Allenes Using an External Chiral Catalyst. / 4.5:
Synthesis of Allenes Using Internal Chiral Auxiliaries. / 4.6:
Kinetic Resolution. / 4.7:
Conclusion. II Special Classes of Allenes. / 4.8:
Allenic Hydrocarbons - Preparation and Use in Organic Synthesis / Henning Hopf.5:
Allenic Hydrocarbons from Simple Building Blocks. / 5.1:
Preparation of Allenic Hydrocarbons. / 5.3:
Allenic Hydrocarbons as Reaction Intermediates. / 5.4:
Why Allenic Hydrocarbons Are of Interest in Preparative Organic Chemistry. / 5.5:
Cyclic Allenes Up to Seven-Membered Rings / Manfred Christl.6:
Three-, Four- and Five-Membered Rings. / 6.1:
Six-Membered Rings. / 6.3:
Seven-Membered Rings. / 6.4:
Acceptor-Substituted Allenes / Klaus Banert ; Jens Lehmann.7:
Synthesis of Acceptor-Substituted Allenes. / 7.1:
Reactions of Acceptor-Substituted Allenes. / 7.3:
Donor-Substituted Allenes / Reinhold Zimmer ; Hans-Ulrich Reissig.7.4:
O-Substituted Allenes. / 8.1:
N-Substituted Allenes. / 8.3:
S- and Se-Substituted Allenes. / 8.4:
Synthesis and Reactions of Allenylmetal Compounds / James A. Marshall ; Benjamin W. Gung ; Melissa L. Grachan.8.5:
Allenyllithium Reagents. / 9.1:
Structure. / 9.2.1:
Allenylcopper Reagents. / 9.3:
Allenylmagnesium Halides. / 9.4:
Allenylboron Reagents. / 9.5:
Allenyltitanium Reagents. / 9.6:
Allenylsilanes. / 9.7:
Allenylstannanes. / 9.8:
Allenylpalladium Reagents. / 9.9:
Allenylzinc Reagents. / 9.10:
Allenylindium Reagents. / 9.11:
Miscellaneous Allenylmetal Reagents. / 9.12:
III Reactions of Allenes. / Volume 2:
Ionic Additions to Allenes / Shengming Ma.10:
Unfunctionalized Allenes. / 10.1:
1,2-Allenyl Sulfides. / 10.2:
1,2-Allenyl Ethers. / 10.4:
1,2-Allenyl Halides. / 10.5:
Phosphorus-Containing Allenes. / 10.6:
1,2- / 10.7:
I Synthesis of Allenes. / Volume 1:
Synthesis of Allenes by Isomerization Reactions / A. Stephen ; K. Hashmi.1:
Introduction. / 1.1:
44.

図書

図書
Kurt Faber
出版情報: Cham : Springer, c2018  xi, 434 p. ; 25 cm
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