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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
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
5.

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
6.

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
7.

図書

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)
8.

図書

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
9.

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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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:
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