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図書
図書
1. Regio- and stereo-controlled oxidations and reductions
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
2.

図書
図書
2. Metal catalysed carbon-carbon bond-forming reactions
edited by Stanley M. Roberts ... [et al.]
出版情報: Chichester : John Wiley, c2004  xvii, 256 p. ; 24 cm
シリーズ名: Catalysts for fine chemical synthesis ; v. 3
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3.

図書
図書
3. Synthesis : carbon with no attached heteroatoms
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
4.

図書
図書
4. Molecular recognition : chemical and biochemical problems II
edited by Stanley M. Roberts
出版情報: Cambridge : Royal Society of Chemistry, c1992  199 p. ; 24 cm
シリーズ名: Special publication / Royal Society of Chemistry ; no. 111
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5.

図書
図書
5. Principles of molecular recognition. 1st ed
edited by A.D. Buckingham, A.C. Legon, and S.M. Roberts
出版情報: London ; New York : Blackie Academic & Professional, 1993  xi, 200 p. ; 24 cm
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6.

電子ブック
ＥＢ
6. Catalysts for Fine Chemical Synthesis: Hydrolysis, Oxidation and Reduction
S. M. Roberts, Geraldine Poignant, Stanley M. Roberts
出版情報: Wiley Online Library - AutoHoldings Books , Chichester : John Wiley & Sons, Inc., 2002
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Series Preface
Preface to Volume 1
Abbreviations
Review / Part I：
The Integration of Biotransformations into the Catalyst Portfolio / 1：
Hydrolysis of esters, amides, nitriles and oxiranes / 1.1：
Reduction reactions / 1.2：
Reduction of carbonyl compounds / 1.2.1：
Reduction of alkenes / 1.2.2：
Oxidative transformations / 1.3：
Carbon-carbon bond-forming reactions / 1.4：
Conclusions / 1.5：
References
Procedures / Part II：
General Information / 2：
Asymmetric Epoxidation / 3：
Introduction / 3.1：
Epoxidation of [alpha], [beta]-Unsaturated Carbonyl Compounds / 4：
Non-asymmetric epoxidation / 4.1：
Asymmetric epoxidation using poly-d-leucine / 4.2：
Synthesis of leucine N-carboxyanhydride / 4.2.1：
Synthesis of immobilized poly-d-leucine / 4.2.2：
Asymmetric epoxidation of (E)-benzylideneacetophenone / 4.2.3：
Conclusion / 4.2.4：
Asymmetric epoxidation using chiral modified diethylzinc / 4.3：
Epoxidation of 2-isobutylidene-1-tetralone / 4.3.1：
Asymmetric epoxidation of (E)-benzylideneacetophenone using the La-(R)-BINOL-Ph[subscript 3]PO/cumene hydroperoxide system / K. Daikai ; M. Kamaura ; J. Inanaga4.3.2：
Merits of the system / 4.4.1：
Epoxidation of Allylic Alcohols / 5：
Asymmetric epoxidation using a chiral titanium complex / 5.1：
Epoxidation of cinnamyl alcohol / 5.2.1：
Epoxidation of (E)-2-methyl-3-phenyl-2-propenol / 5.2.2：
Epoxidation of (E)-2-hexen-1-ol / 5.2.3：
Asymmetric epoxidation of (E)-undec-2-en-1-ol using poly(octamethylene tartrate) / D.C. Sherrington ; J.K. Karjalainen ; O.E.O. Hormi5.2.4：
Synthesis of branched poly (octamethylene-L-(+)-tartrate) / 5.3.1：
Asymmetric epoxidation of (E)-undec-2-en-1-ol / 5.3.2：
Epoxidation of Unfunctionalized Alkenes and [alpha], [beta]-Unsaturated Esters / 6：
Asymmetric epoxidation of disubstituted Z-alkenes using a chiral salen-manganese complex / 6.1：
Epoxidation of (Z)-methyl styrene / 6.1.1：
Epoxidation of (Z)-ethyl cinnamate / 6.1.2：
Asymmetric epoxidation of disubstituted E-alkanes using a D-fructose based catalyst / 6.1.3：
Epoxidation of (E)-stilbene / 6.2.1：
Enantioselective epoxidation of (E)-[beta]-methylstyrene by D[subscript 2]-symmetric chiral trans-dioxoruthenium (VI) porphyrins / Rui Zhang ; Wing-Yiu Yu ; Chi-Ming Che6.2.2：
Preparation of the trans-dioxoruthenium (VI) complexes with D[subscript 2]-symmetric porphyrins (H[subscript 2]L[superscript 1-3]) / 6.3.1：
Enantioselective epoxidation of (E)-[beta]-methylstyrene / 6.3.2：
Asymmetric Hydroxylation and Aminohydroxylation / 6.3.3：
Asymmetric aminohydroxylation of 4-methoxystyrene / P.O'Brien ; S.A. Osborne ; D.D. Parker7.1：
Asymmetric dihydroxylation of (1-cyclohexenyl)acetonitrile / Jean-Michel Vatele7.1.1：
(R,R)-(1,2-Dihydroxycyclohexyl)acetonitrile acetonide / 7.2.1：
Asymmetric Sulfoxidation / 7.2.2：
Asymmetric oxidation of sulfides and kinetic resolution of sulfoxides / Laura Palombi ; Arrigo Scettri8.1：
Asymmetric oxidation of 4-bromothioanisole / 8.1.1：
Kinetic resolution of racemic 4-bromophenyl methyl sulfoxide / 8.1.2：
Asymmetric Reduction of Ketones Using Organometallic Catalysts / 9：
Asymmetric hydrogenation using a metal catalyst: [Ru((S)-BiNAP)] / 9.1：
Asymmetric transfer hydrogenation of [beta]-ketoesters / Kathelyne Everaere ; Jean-Francois Carpentier ; Andre Mortreux ; Michel Bulliard9.3：
(S,S)-1,2-bis(tert-Butylmethylphosphino)ethane (BisP*): Synthesis and use as a ligand / T. Imamoto9.4：
Synthesis of BisP* / 9.4.1：
Synthesis of 1,2-bis(tert-butylmethylphosphino) ethaneruthenium bromide (BisP*-Ru) / 9.4.2：
Synthesis of (R)-(-)-methyl 3-hydroxypentanoate using (BisP*-Ru) / 9.4.3：
(1S,3R,4R)-2-Azanorbornylmethanol, an efficient ligand for ruthenium-catalysed asymmetric transfer hydrogenation of aromatic ketones / Diego A. Alonso ; Pher G. Andersson9.5：
Synthesis of ethyl(1S,3R,4R)-2-[(S)-1-phenylethylamino]-2-azabicyclo[2.2.1] hept-5-ene-3-carboxylate / 9.5.1：
Synthesis of (1S,3R,4R)-3-hydroxymethyl-2-azabicyclo[2.2.1]heptane / 9.5.2：
Ruthenium-catalysed asymmetric transfer hydrogenation of acetophenone / 9.5.3：
Asymmetric Reduction of Ketones Using Bakers' Yeast / 10：
Bakers' yeast reduction of ethyl acetoacetate / 10.1：
Enantioselective synthesis of cis-N-carbobenzyloxy-3-hydroxyproline ethyl ester / Mukund P. Sibi ; James W. Christensen10.2：
Immobilization of bakers' yeast / 10.2.1：
Bakers' yeast reduction of cis-N-carbobenzyloxy-3-ketoproline ethyl ester / 10.2.2：
Asymmetric Reduction of Ketones Using Nonmetallic Catalysts / 11：
Oxazaborolidine borane reduction of acetophenone / 11.1：
Oxazaphosphinamide borane reduction of chloroacetophenone / 11.3：
Asymmetric reduction of chloroacetophenone using a sulfoximine catalyst / 11.4：
Preparation of [beta]-hydroxysulfoximine borane / 11.4.1：
Reduction of chloroacetophenone using the sulfoximine borane / 11.4.2：
Summary / 11.4.3：
Asymmetric reduction of bromoketone catalysed by cis-aminoindanol oxazaborolidine / Chris H. Senanayake ; H. Scott Wilkinson ; Gerald J. Tanoury11.5：
Synthesis of aminoindanol oxazaborolidine / 11.5.1：
Asymmetric reduction of 2-bromo-(3-nitro-4-benzyloxy)acetophenone / 11.5.2：
Stereoselective reduction of 2,3-butadione monoxime trityl ether / 11.5.3：
Stereoselective reduction of methyl 3-oxo-2-trityloxyiminostearate / 11.5.5：
Stereoselective reduction of 1-(tert-butyldimethylsilyloxy)-3-oxo-2-trityloxyiminooctadecane / 11.5.6：
Enantioselective reduction of ketones using N-arylsulfonyl oxazaborolidines / Pingrong Liu ; Gregory R. Cook11.6：
Synthesis of N-(2-pyridinesulfonyl)-1-amino-2-indanol / 11.6.1：
Asymmetric reduction of a prochiral ketone (chloroacetophenone) / 11.6.2：
Reduction of ketones using amino acid anions as catalyst and hydrosilane as oxidant / Michael A. Brook11.7：
Asymmetric Hydrogenation of Carbon-Carbon Double Bonds Using Organometallic Catalysts / 12：
Hydrogenation of dimethyl itaconate using [Rh((S,S)-Me-BPE)] / 12.1：
Hydrogenation of an [alpha]-amidoacrylate using [Rh((R,R)-Me-DuPHOS)] / 12.3：
Hydrogenation of an [alpha]-amidoacrylate using [Rh(B[3.2.0]DPO)] complexes / 12.4：
Preparation of (COD)[subscript 2] Rh[superscript +]BF[subscript 4 superscript -] / 12.4.1：
Preparation of the bisphosphinite ligand / 12.4.2：
Asymmetric reduction of [alpha]-acetamido cinnamic acid / 12.4.3：
Hydrogenation of enol carbonates and 4-methylene-N-acyloxazolidinone using [Rh((R)-BiNAP)] complexes / P.H. Dixneuf ; C. Bruneau ; P. Le Gendre12.5：
Synthesis of (S)-4,4,5-trimethyl-1, 3-dioxolane-2-one / 12.5.1：
Synthesis of (S)-2-methyl-2,3-butanediol / 12.5.2：
Preparation of optically active N-acyloxazolidinones / 12.5.3：
Synthesis of (R)-N-propionyl-4,5,5-trimethyl-1, 3-oxazolidin-2-one / 12.5.4：
Enantioselective ruthenium-catalyzed hydrogenation of vinylphosphonic acids / Virginie Ratovelomanana-Vidal ; Jean-Pierre Genet12.6：
Synthesis of chiral Ru(II) catalysts / 12.6.1：
Asymmetric hydrogenation of vinylphosphonic acids carrying a phenyl substituent at C[subscript 2] / 12.6.2：
Asymmetric reduction of a vinylphosphonic acid carrying a naphthyl substituent at C[superscript 2] / 12.6.3：
Scope of the hydrogenation reaction / 12.6.4：
Synthesis of a cylindrically chiral diphosphine and asymmetric hydrogenation of dehydroamino acids / Jahyo Kang ; Jun Hee Lee12.7：
Preparation of (R,R)-1,1'-bis([alpha]-hydroxypropyl) ferrocene / 12.7.1：
Preparation of (R,R)-1,1'-bis [alpha-(dimethylamino)propyl]ferrocene / 12.7.2：
Preparation of (R,R,[subscript p]S,[subscript p]S)-1,1'-bis [alpha-(dimethylamino)propyl]-2,2'-bis (diphenyl-phosphino)ferrocene / 12.7.3：
Preparation of (R,R,[subscript p]S,[subscript p]S)-1,1'-bis [alpha-acetoxypropyl)-2,2'-bis(diphenyl-phosphino)ferrocene / 12.7.4：
Preparation of ([subscript p]S,[subscript p]S)-1, 1'-bis (diphenylphosphino)-2,2'-bis(1-ethylpropyl) ferrocene [(S,S)-3-Pt-FerroPHOS] / 12.7.5：
Preparation of [(COD)Rh(([subscript p]S, [subscript p]S)-1, 1'-bis(diphenylphosphino)-2,2'-bis (1-ethylpropyl)ferrocene superscript +]BF[superscript - subscript 4] / 12.7.6：
Asymmetric hydrogenation of [alpha]-acetamido cinnamic acid / 12.7.7：
Synthesis and application of diamino FERRIPHOS as ligand for enantioselective Rh-catalysed preparation of chiral [alpha]-amino acids / Matthias Lotz ; Juan J. Almena Perea ; Paul Knochel12.8：
Synthesis of 1,1'-di(benzoyl)ferrocene / 12.8.1：
Synthesis of (S,S)-1,1'-bis ([alpha]-hydroxyphenylmethyl)ferrocene / 12.8.2：
Synthesis of (S,S)-1,1'-bis ([alpha]-acetoxyphenylmethyl)ferrocene / 12.8.3：
Synthesis of (S,S)-1,1'-bis([alpha]-N,N-dimethylaminophenylmethyl)ferrocene / 12.8.4：
Synthesis of ([alpha]S, [alpha]'S)-1,1'-bis([alpha]-N, N-dimethylaminophenylmethyl)-(R,R)-1,1'bis(diphenylphosphino)ferrocene / 12.8.5：
Asymmetric hydrogenation of methyl-(Z)-3-phenyl-2-methyl-carboxamido-2-propenoate using (S)-(R)-diamino FERRIPHOS as chiral ligand / 12.8.6：
Employment of Catalysts Working in Tandem / 13：
A one-pot sequential asymmetric hydrogenation utilizing Rh(I)- and Ru(II)-catalysts / Takayuki Doi ; Takashi Takahashi13.1：
Synthesis of ethyl (Z)-4-acetamido-3-oxo-5-phenyl-4-pentenoate / 13.1.1：
Asymmetric hydrogenation of ethyl 4-acetamido-3-oxo-5-phenyl-4-pentenoate / 13.1.2：
Index
Series Preface
Preface to Volume 1
Abbreviations
7.

電子ブック
ＥＢ
7. Catalysts for Fine Chemical Synthesis: Metal Catalysed Carbon-Carbon Bond-Forming Reactions
Stanley M. Roberts
出版情報: Wiley Online Library - AutoHoldings Books , John Wiley & Sons, Inc., 2004
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目次情報: 続きを見る
Series Preface
Preface to Volume 3
Abbreviations
List of Chemical Names Used
Considerations of Industrial Fine Chemical Synthesis / Mark W. Hooper1：
Introduction / 1.1：
Types of processes - flow charts / 1.2：
Costs associated with use of catalysts / 1.3：
Alkylation and Allylation Adjacent to a Carbonyl Group / 2：
The RuH 2 (CO)(PPh 3 ) 3 -catalysed alkylation, alkenylation and arylation of aromatic ketones via carbon-hydrogen bond cleavage / Fumitoshi Kakiuchi ; Satoshi Ueno ; Naoto Chatani2.1：
Catalytic, asymmetric synthesis of a,a-disubstituted amino acids using a chiral copper-salen complex as a phase transfer catalyst / Michael North ; Jose A. Fuentes2.2：
Asymmetric phase-transfer catalysed alkylation of glycine imines using cinchona alkaloid derived quaternary ammonium salts / Barry Lygo ; Benjamin I. Andrews2.3：
Asymmetric Alkylation or Amination of Allylic Esters / 3：
Synthesis and application in palladium-catalysed asymmetric allylic substitution of enantiopure cyclic ++-iminophosphine ligands / Maria Zablocka ; Marek Koprowski ; Jean-Pierre Majoral ; Mathieu Achard ; G+,rard Buono3.1：
(9H,9'H,10H,10'H,11H,11H',13H,13'H,14H,14'H,15H,15'Hperfluorotricosane-12,12'-diyl)bis[(4S)-4-phenyl-2-oxazoline as a ligand for asymmetric palladium-catalysed alkylation of allylic acetates in fluorous media / J+,r+&me Bayardon ; Denis Sinou3.2：
Facile synthesis of new axially chiral diphosphine complexes for asymmetric catalysis / Matthias Lotz ; Gernot Kramer ; Katja Tappe ; Paul Knochel3.3：
Chiral ferrocenyl-imino phosphines as ligands for palladium-catalysed enantioselective allylic alkylations / Pierluigi Barbaro ; Claudio Bianchini ; Giuliano Giambastiani ; Antonio Togni3.4：
Suzuki Coupling Reactions / 4：
Palladium-catalysed borylation and Suzuki coupling (BSC) to obtain ++-benzo[b]thienyldehydroamino acid derivatives / Ana S. Abreu ; Paula M. T. Ferreira ; Maria-Jo+zo R. P. Queiroz4.1：
Palladium-catalysed cross-coupling reactions of 4-tosylcoumarins and arylboronic acids: synthesis of 4-arylcoumarin compounds / Jie Wu ; Lisha Wang ; Reza Fathi ; Zhen Yang4.2：
Cyclopropyl arenes, alkynes and alkenes from the in situ generation of B-cyclopropyl-9-BBN and the Suzuki-Miyaura coupling of aryl, alkynyl and alkenyl bromides / Ramon E. Huertas ; John A. Soderquist4.3：
One-pot synthesis of unsymmetrical 1,3-dienes through palladium-catalysed sequential borylation of a vinyl electrophile by a diboron and cross-coupling with a distinct vinyl electrophile / Tatsuo Ishiyama ; Norio Miyaura4.4：
Pd(OAc) 2 /2-Aryl oxazoline catalysed Suzuki coupling reactions of aryl bromides and boronic acids / Bin Tao ; David W. Boykin4.5：
Palladium-catalysed reactions of haloaryl phosphine oxides: modular routes to functionalised ligands / Colin Baillie ; Lijin Xu ; Jianliang Xiao4.6：
Bulky electron rich phosphino-amines as ligands for the Suzuki coupling reaction of aryl chlorides / Matthew L. Clarke ; J. Derek Woollins4.7：
Arylation of ketones, aryl amination and Suzuki-Miyaura cross coupling using a well-defined palladium catalyst bearing an N-heterocyclic carbene ligand / Nicholas Marion ; Oscar Navarro ; Roy A. Kelly III ; Steven P. Nolan4.8：
Heck Coupling Reactions / 5：
Palladium-catalysed multiple and asymmetric arylations of vinyl ethers carrying co-ordinating nitrogen auxiliaries: synthesis of arylated ketones and aldehydes / Peter Nilsson ; Mats Larhed5.1：
Palladium-catalysed highly regioselective arylation of electron-rich olefins / Jun Mo5.2：
1-[4-(S)-tert-Butyl-2-oxazolin-2-yl]-2-(S)-(diphenylphosphino) ferrocene as a ligand for the palladium-catalysed intermolecular asymmetric Heck reaction of 2,3-dihydrofuran / Tim G. Kilroy ; Yvonne M. Malone ; Patrick J. Guiry5.3：
Sonogashira Coupling Reactions / 6：
Nonpolar biphasic catalysis: Suzuki- and Sonogashira coupling reactions / Anupama Datta ; Herbert Plenio6.1：
Polystyrene-supported soluble palladacycle catalyst as recyclable catalyst for H<$$$> / 6.2：
Series Preface
Preface to Volume 3
Abbreviations
8.

電子ブック
ＥＢ
8. Catalysts for Fine Chemical Synthesis: Microporous and Mesoporous Solid Catalysts
Eric G. Derouane, E. G. Derouane, Stanley M. Roberts
出版情報: Wiley Online Library - AutoHoldings Books , Chichester : John Wiley & Sons, Inc., 2007
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Series Preface
Preface to Volume 4
Abbreviations
An Overview of Zeolite, Zeotype and Mesoporous Solids Chemistry: Design, Synthesis and Catalytic Properties / Thomas Maschmeyer ; Leon van de Water1：
Zeolites, zeotypes and mesoporous solids: synthetic aspects / 1.1：
Introduction / 1.1.1：
Synthetic aspects: template theory for zeolite synthesis / 1.1.2：
Synthetic aspects: template theory for mesoporous oxides synthesis / 1.1.3：
Design of extra-large pore zeolites and other micro- and mesoporous catalysts / 1.2：
Extra-large pore zeolites / 1.2.1：
Hierarchical pore architectures: combining micro- and mesoporosity / 1.2.3：
Potential of post-synthesis functionalized micro- and mesoporous solids as catalysts for fine chemical synthesis / 1.3：
Covalent functionalization / 1.3.1：
Noncovalent immobilization approaches / 1.3.3：
Single-site catalysts inspired by natural systems / 1.3.4：
References
Problems and Pitfalls in the Applications of Zeolites and other Microporous and Mesoporous Solids to Catalytic Fine Chemical Synthesis / Michel Guisnet ; Matteo Guidotti2：
Zeolite catalysed organic reactions / 2.1：
Fundamental and practical differences with homogeneous reactions / 2.2.1：
Batch mode catalysis / 2.2.2：
Continuous flow mode catalysis / 2.2.3：
Competition for adsorption: influence on reaction rate, stability and selectivity / 2.2.4：
Catalyst deactivation / 2.2.5：
General conclusions / 2.3：
Aromatic Acetylation / 3：
Aromatic acetylation / 3.1：
Acetylation with Acetic Anhydride / 3.1.1：
Acetylation with Acetic Acid / 3.1.2：
Procedures and protocols / 3.2：
Selective synthesis of acetophenones in batch reactors through acetylation with acetic anhydride / 3.2.1：
Selective synthesis of acetophenones in fixed bed reactors through acetylation with acetic anhydride / 3.2.2：
Aromatic Benzoylation / Patrick Geneste ; Annie Finiels4：
Aromatic benzoylation / 4.1：
Effect of the zeolite / 4.1.1：
Effect of the acylating agent / 4.1.2：
Effect of the solvent / 4.1.3：
Benzoylation of phenol and the Fries rearrangement / 4.1.4：
Kinetic law / 4.1.5：
Substituent effect / 4.1.6：
Experimental / 4.1.7：
Acylation of anisole over mesoporous aluminosilicates / 4.2：
Nitration of Aromatic Compounds / Avelino Corma ; Sara Iborra5：
Reaction mechanism / 5.1：
Nitration of aromatic compounds using zeolites as catalysts / 5.3：
Nitration in liquid phase / 5.3.1：
Vapour phase nitration / 5.3.2：
Conclusions / 5.4：
Oligomerization of Alkenes / 6：
Reaction mechanisms / 6.1：
Acid zeolites as catalysts for oligomerization of alkenes / 6.3：
Medium pore zeolites: influence of crystal size and acid site density / 6.3.1：
Use of large pore zeolites / 6.3.2：
Catalytic membranes for olefin oligomerization / 6.3.3：
Mesoporous alominosilicates as oligomerization catalysts / 6.4：
Nickel supported aluminosilicates as catalysts / 6.5：
Microporous and Mesoporous Catalysts for the Transformation of Carbohydrates / Claude Moreau7：
Hydrolysis of sucrose in the presence of H-form zeolites / 7.1：
Hydrolysis of fructose and glucose precursors / 7.3：
Isomerization of glucose into fructose / 7.4：
Dehydration of fructose and fructose-precursors / 7.5：
Dehydration of xylose / 7.6：
Synthesis of alkyl-D-glucosides / 7.7：
Synthesis of butyl-D-glucosides / 7.7.1：
Synthesis of long-chain alkyl-D-glucosides / 7.7.2：
Synthesis of alkyl-D-fructosides / 7.8：
Hydrogenation of glucose / 7.9：
Oxidation of glucose / 7.10：
One-pot Reactions on Bifunctional Catalysts / 7.11：
Examples / 8.1：
One-pot transformations involving successive hydrogenation and acid-base steps / 8.2.1：
One-pot transformations involving successive oxidation and acid-base steps / 8.2.2：
Base-type Catalysts / Didier Tichit ; Daniel Brunel9：
Characterization of solid bases / 9.1：
Test reactions / 9.2.1：
Probe molecules combined with spectroscopic methods / 9.2.2：
Solid base catalysts / 9.3：
Alkaline earth metal oxides / 9.3.1：
Catalysis on alkaline earth metal oxides / 9.3.2：
Hydrotalcites and related compounds / 9.3.3：
Organic base-supported catalysts / 9.3.4：
Hybrid Oxidation Catalysts from Immobilized Complexes on Inorganic Microporous Supports / Dirk De Vos ; Ive Hermans ; Ben Sels ; Pierre Jacobs9.4：
Introduction and scope / 10.1：
Oxygenation potential of heme-type complexes in zeolite / 10.2：
Metallo-phthallocyanines encapsulated in the cages of faujasite-type zeolites / 10.2.1：
Oxygenation potential of metallo-phthallocyanines encapsulated in the mesopores of VPI-5 AIPO[subscript 4] / 10.2.2：
Oxygenation potential of zeolite encapsulated metallo-porphyrins / 10.2.3：
Oxygenation potential of zeolite encapsulated nonheme complexes / 10.3：
Immobilization of N,N[prime]-bidentate complexes in zeolite Y / 10.3.1：
Ligation of zeolite exchanged transition ions with bidentate aza ligands / 10.3.2：
Ligation of zeolite exchanged transition ions with tri- and tetra-aza(cyclo)alkane ligands / 10.3.3：
Ligation of zeolite exchanged transition ions with Schiff base-type ligands / 10.3.4：
Zeolite effects with N,N[prime]-bis(2-pyridinecarboxamide) complexes of Mn and Fe in zeolite Y / 10.3.5：
Zeolite encapsulated chiral oxidation catalysts / 10.3.6：
Acknowledgements / 10.4：
Subject Index
Mesoporous aluminosilicates as oligomerization catalysts
Base-type Catalysis
Series Preface
Preface to Volume 4
Abbreviations
9.

図書
図書
9. Recent advances in the chemistry of [Beta]-Lactam antibiotics : the proceedings of the third international symposium, arranged by the Fine Chemicals and Medicinals Group of the Industrial Division of the Royal Society of Chemistry, Cambridge, England, 2nd-4th July 1984 (pbk.)
edited by A.G. Brown, S.M. Roberts
出版情報: London : Royal Society of Chemistry, c1985  viii, 391 p. ; 21 cm
シリーズ名: Special publication / Royal Society of Chemistry ; no. 52
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10.

図書
図書
10. Molecular recognition : chemical and biochemical problems : the proceedings of an international symposium, University of Exeter, April 1989
edited by Stanley M. Roberts
出版情報: Cambridge : Royal Society of Chemistry, c1989  xi, 285 p. ; 21 cm
シリーズ名: Special publication / Royal Society of Chemistry ; no. 78
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