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1.

図書
図書
1. 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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2.

図書
図書
2. Catalysis by polyoxometalates
Ivan Kozhevnikov
出版情報: Chichester : J. Wiley & Sons, c2002  xiv, 201 p. ; 24 cm
シリーズ名: Catalysts for fine chemical synthesis ; v. 2
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目次情報: 続きを見る
Series Preface
Preface to Volume 2
Introduction / 1：
Scope and definitions / 1.1：
Nomenclature / 1.2：
Historical background / 1.3：
Introduction to catalysis by polyoxometalates / 1.4：
References
Properties of Polyoxometalates / 2：
Structures of polyoxometalates / 2.1：
General principles / 2.1.1：
The Keggin structure / 2.1.2：
The Wells-Dawson structure / 2.1.3：
The Anderson-Evans structure / 2.1.4：
The Dexter-Silverton structure / 2.1.5：
Crystal structure of heteropoly compounds / 2.2：
Thermal stability / 2.3：
Solubility / 2.4：
Formation and state in solution / 2.5：
Stability of polyoxometalates in solution / 2.5.1：
Polyoxometalates as ligands / 2.5.2：
Isotope exchange / 2.5.3：
Kinetics and mechanism of substitution in polyoxmetalates / 2.5.4：
Acid properties / 2.6：
Proton structure / 2.6.1：
Heteropoly acids in solutions / 2.6.2：
Acidity of solid heteropoly acids / 2.6.3：
Redox properties / 2.7：
Synthesis of Polyoxometalates / 3：
General methods of synthesis / 3.1：
Keggin polyoxometalates / 3.2：
12-Molybdosilicic acid, [alpha]-H[subscript 4 SiMo[subscript 12]O[subscript 40] / 3.2.1：
12-Tungstosilicic acid, [alpha]-H[subscript 4 SiW[subscript 12]O[subscript 40] / 3.2.2：
12-Tungstophosphoric acid, [alpha]-H[subscript 3 PW[subscript 12]O[subscript 40] / 3.2.3：
12-Molybdophosphoric acid, [alpha]-H[subscript 3 PMo[subscript 12]O[subscript 40] / 3.2.4：
12-Tungstogermanic acid, [alpha]-[H[subscript 4 GeW[subscript 12]O[subscript 40] / 3.2.5：
11-Molybdo-1-vanadophosphoric acid, H[subscript 4 PMo[subscript 11] VO[subscript 40] / 3.2.6：
10-Molybdo-2-vanadophosphoric acid, H[subscript 5 PMo[subscript 10]V[subscript 2]O[subscript 40] / 3.2.7：
9-Molybdo-3-vanadophosphoric acid, H[subscript 6 PMo[subscript 9] V[subscript 3]O[subscript 40] / 3.2.8：
Transition-metal-substituted tungstophosphates, {PW[subscript 11]MO[subscript 39]} / 3.2.9：
Wells-Dawson polyoxometalates / 3.3：
18-Tungstodiphosphoric acid, H[subscript 6 P[subscript 2]W[subscript 18]O[subscript 62] / 3.3.1：
Sandwich-type polyoxometalates / 3.4：
Na[subscript 12 WZn[subscript 3](H[subscript 2]O)[subscript 2](ZnW[subscript 9]O[subscript 34])[subscript 2] / 3.4.1：
Na[subscript 12 WCo[subscript 3 superscript II](H[subscript 2]O)[subscript 2] (Co[superscript II]W[subscript 9]O[subscript 34])[subscript 2] / 3.4.2：
K[subscript 11 WZnRu[subscript 2 superscript III](OH)(H[subscript 2]O) (ZnW[subscript 9]O[subscript 34])[subscript 2] / 3.4.3：
K[subscript 10 WZnRh[superscript III subscript 2](H[subscript 2]O)(ZnW[subscript 9]O[subscript 34])[subscript 2] / 3.4.4：
Peroxo polyoxometalates / 3.5：
Venturello complex, {PO[subscript 4 WO(O[subscript 2])[subscript 2 subscript 4]}[superscript 3-] / 3.5.1：
Polyoxometalate catalysts / 3.6：
Solid acid catalysts / 3.6.1：
Homogeneous catalysts / 3.6.2：
Acid Catalysis by Heteropoly Compounds / 4：
General overview / 4.1：
The scope of applications / 4.1.1：
Mechanistic principles / 4.1.2：
Homogeneous acid catalysis / 4.2：
Acid-catalysed reactions / 4.2.1：
Acid-catalysed reactions in biphasic liquid-liquid systems / 4.3：
Biphasic reactions / 4.3.1：
Heterogeneous acid catalysts / 4.4：
Heteropoly acid catalysts / 4.4.1：
Heterogeneous catalysis in liquid-solid systems / 4.4.2：
Heterogeneous catalysis in gas-solid systems / 4.4.3：
Deactivation and regeneration of solid heteropoly acid catalysts / 4.5：
Polyoxometalates as Catalysts for Selective Oxidation / 5：
Liquid-phase oxidation / 5.1：
Oxidation with dioxygen / 5.1.1：
Oxidation with hydrogen peroxide / 5.1.2：
Oxidation with organic peroxides / 5.1.3：
Miscellaneous oxidations / 5.1.4：
Gas-phase oxidation / 5.2：
Oxidation catalysts / 5.2.1：
Reactions / 5.2.3：
Miscellaneous Catalytic Applications of Polyoxometalates / 6：
Hydrogenation, carbonylation and related reactions / 6.1：
Polyanion-stabilised clusters / 6.2：
Polyoxometalates as catalyst precursors / 6.3：
Catalysis by Polyoxometalates in Industry / 7：
Acid catalysis / 7.1：
Hydration of olefins / 7.1.1：
Synthesis of ethyl acetate from ethylene and acetic acid / 7.1.2：
Selective oxidation / 7.2：
Oxidation of methacrolein in methacrylic acid / 7.2.1：
Oxidation of ethylene to acetic acid / 7.2.2：
Other Applications of Polyoxometalates / 8：
Analytical chemistry / 8.1：
Elemental analysis / 8.1.1：
Analysis of biomaterials / 8.1.2：
Separation / 8.2：
Processing of radioactive waste / 8.2.1：
Sorption of gases / 8.2.2：
Corrosion-resistant coatings / 8.3：
Polyoxometalates as additives to inorganic and organic matrices / 8.4：
Additives in sol-gel matrices / 8.4.1：
Additives in polymer matrices / 8.4.2：
Membranes / 8.5：
Fuel cells / 8.5.1：
Selective electrodes / 8.5.2：
Gas sensors / 8.5.3：
Polyoxometalates in medicine: antiviral and antitumoral activity / 8.6：
Index
Series Preface
Preface to Volume 2
Introduction / 1：
3.

図書
図書
3. Hydrolysis, oxidation and reduction
edited by Stan M. Robert and Geraldine Poignant
出版情報: Chichester : J. Wiley & Sons, c2002  xviii, 225 p. ; 24 cm
シリーズ名: Catalysts for fine chemical synthesis ; v. 1
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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
4.

図書
図書
4. Fine chemicals through heterogeneous catalysis
[edited by] Roger Arthur Sheldon, Herman van Bekkum
出版情報: Weinheim ; New York : Wiley-VCH, c2001  xxv, 611 p. ; 25 cm
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5.

図書
図書
5. Catalysis for Renewables : From Feedstock to Energy Production (hdk)
Hrsg. Gabriele Centi ; Hrsg. Rutger A. van Santen
出版情報: Weinheim : WILEY-VCH, c2007  xxiii, 423 p ; 25 cm
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6.

図書
図書
6. Catalysis from A to Z : a concise encyclopedia. 3., completely rev. and enl. ed ([set] - Vol. 3. O to Z)
edited by Boy Cornils ... [et al.]
出版情報: Weinheim : Wiley-VCH-Verl, 2007  3 v. ; 25 cm
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目次情報: 続きを見る
Topics Included: catalysts - heterogeneous, homogeneous, acid, base ligands
Biocatalysis catalytic reactions in organic synthesis kinetics and thermodynamics of catalytic reactions
Catalyst labelling theoretical backgrounds of catalytic reactions
Industrial catalytic processes stereoselective catalysis autoclaves colloids nanomaterials
Spectroscopical methods for catalyst analysis radicals enzymatic catalysis vitamins
Topics Included: catalysts - heterogeneous, homogeneous, acid, base ligands
Biocatalysis catalytic reactions in organic synthesis kinetics and thermodynamics of catalytic reactions
Catalyst labelling theoretical backgrounds of catalytic reactions
7.

電子ブック
ＥＢ
7. 触媒化学 (: electronic bk)
上松敬禧 [ほか] 著
出版情報: Boulder : NetLibrary, 2008  1オンラインリソース
シリーズ名: 応用化学シリーズ ; 6
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