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1.

図書

図書
edited by Robert M. Coates and Scott E. Denmark
出版情報: Chichester : John Wiley & Sons, c1999  xvi, 746 p. ; 29 cm
シリーズ名: Handbook of reagents for organic synthesis ; [1]
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Partial table of contents
Classes
Acetylenes and Allenes
Aluminum and Boron Reagents
Reagents
Enolates, Homoenolates, and Dicarbonyl Compounds
Epoxides
Halo Compounds
Transition Metal and Lanthanide Reagents
Zinc Reagents
Acetyl Chloride
Acetylene
Acrylonitrile
Allenylboronic Acid
Benzenediazonium Tetrafluoroborate
1,4-Benzoquinone
9-Borabicyclo[3.3.1]nonane Dimer
2-(2-Bromoethyl)-1,3-dioxane
Bromoform
Chlorosulfonyl Isocyanate
Chlorotrimethylsilane
Diethyl Malonate
Diethylzinc
Dimethylformamide Diethyl Acetal
Dimethyl(methylene)ammonium Iodide
Epichlorohydrin
Ethoxyacetylene
3-Hydroxyisoborneol
Iodoform
Iodomethane
Mandelic Acid
Manganese(III) Acetate
Methylcopper-Boron Trifluoride Etherate
Methyl Cyanoformate
Potassium Cyanide
Propargyl Chloride
Triethylaluminum
Triethylborane
Vinyltributylstannane
Zinc-Copper Couple
List of Contributors
Indexes
Partial table of contents
Classes
Acetylenes and Allenes
2.

図書

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

図書

図書
edited by Steven D. Burke and Rick L. Danheiser
出版情報: Chichester : John Wiley & Sons, c1999  viii, 550 p. ; 29 cm
シリーズ名: Handbook of reagents for organic synthesis ; [2]
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Partial table of contents
Aluminum Amalgam
Aluminum Hydride
Borane-Tetrahydrofuran
Bromine
Chromium(II) Chloride
Chromium(VI) Oxide
Hydrogen Sulfide
Iodosylbenzene
Lithium-Ethylamine
Lithium Naphthalenide
Manganese Dioxide
Mercury(II) Oxide
Palladium on Carbon
Palladium(II) Hydroxide on Carbon
Peracetic Acid
Rhodium on Alumina
Ruthenium Catalysts
Ruthenium(VIII) Oxide
Sodium-Alcohol
Sodium Amalgam
Sodium-Ammonia
Sulfur
Thallium(III) Nitrate Trihydrate
Thallium(III) Trifluoroacetate
Thexylborane
Zinc
Zinc Borohydride
Zinc/Copper Couple
List of Contributors
Indexes
Partial table of contents
Aluminum Amalgam
Aluminum Hydride
4.

図書

図書
edited by Hans J. Reich and James H. Rigby
出版情報: Chichester : John Wiley & Sons, c1999  xii, 494 p. ; 29 cm
シリーズ名: Handbook of reagents for organic synthesis ; [3]
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Preface
Introduction
Organic Synthesis Examples
Recent Review Articles and Monographs
A-Z list of Reagents
List of Contributors
Reagent Formula Index
Subject Index
Preface
Introduction
Organic Synthesis Examples
5.

図書

図書
edited by Anthony J. Pearson and William R. Roush
出版情報: Chichester : John Wiley & Sons, c1999  xii, 513 p. ; 29 cm
シリーズ名: Handbook of reagents for organic synthesis ; [4]
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Partial table of contents
Acetic Anhydride
Acetyl Chloride (+ co-reactants)
Aluminum Chloride
Boron Trifluorideetherate
Bromodimethylborane
2,2-Dimethyl-1,3-propanediol
Dimethyl Sulfate
Diphenylbis(1,1,1,3,3,3-hexafluoro-2-phenyl-2-propoxy)-sulfirane
Ethylaluminum Dichloride
N-Ethylbenzisoxazolium Tetrafluoroborate
Hydrazine
1-Hydroxybenzotriazole
Lithium Bromide
Lithium Chloride
Lithium Iodide
Montmorillonite K-10
2-Morpholinoethyl Isocyanide
Phenyl Phosphorodi(1-imidazolate)
Phosgene
1,3-Propanediol
1,3-Propanedithiol
Silver(I) Tetrafluoroborate
Triethylaluminum
Triethyl Orthoformate
Trifluoroacetic Anhydride
Zinc Bromide
Zinc Chloride
Zinc Iodide
Zinc Bis(p-toluenesulfonate)
List of Contributors
Indexes
Partial table of contents
Acetic Anhydride
Acetyl Chloride (+ co-reactants)
6.

図書

図書
by Richard C. Larock
出版情報: New York : Wiley-VCH, c1999  xliii, 2583 p. ; 26 cm
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目次情報:
Quick-Start Instructions
Personalizing the COT Infobase
Searching the COT Infobase
Quick-Start Instructions
Personalizing the COT Infobase
Searching the COT Infobase
7.

図書

図書
Tse-Lok Ho
出版情報: River Edge, NJ : World Scientific, 1998  xi, 386 p. ; 23 cm
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8.

図書

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

図書

図書
[edited by] Matthias Beller, Carsten Bolm
出版情報: Weinheim ; Chichester : Wiley-VCH, c1998  2 v. ; 25 cm
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Preface.
General. / 1:
Basic Aspects of Organic Synthesis with Transition Metals (Barry M. Trost). / 1.1:
Concepts for the Use of Transition Metals in Industrial Fine Chemical Synthesis (Wilhelm Keim). / 1.2:
Transition Metal-Catalyzed Reactions. / 2:
Hydroformylation: Applications in the Synthesis of Pharmaceuticals and Fine Chemicals (Matthias Beller and Kamal Kumar). / 2.1:
New Synthetic Applications of Tandem Reactions under Hydroformylation Conditions (Peter Eilbracht and Axel M. Schmidt). / 2.2:
Multiple Carbon-Carbon Bond Formations under Hydroformylation Conditions (Peter Eilbracht and Axel M. Schmidt). / 2.3:
Hydrocarboxylation and Hydroesterification Reactions Catalyzed by Transition Metal Complexes (Bassam El Ali and Howard Alper). / 2.4:
The Amidocarbonylation of Aldehydes (Axel Jacobi von Wangelin, Helfried Neumann, Dirk Gordes, and Matthias Beller). / 2.5:
Transition Metal-catalyzed Alkene and Alkyne Hydrocyanations (Albert L. Casalnuovo and T.V. Rajan Babu). / 2.6:
Cyclopropanation (Andreas Pfaltz). / 2.7:
Cyclomerization of Alkynes (H. Bonnemann and W. Brijoux). / 2.8:
Coupling of Aryl and Alkyl Halides with Organoboron Reagents (Suzuki Reaction) (Alexander Zapf). / 2.9 Isomerization of Olefin and the Related Reactions (Sei Otsuka and Kazuhide Tani).:
Transition Metal-Catalyzed Arylation of Amines and Alcohols (Alexander Zapf, Matthias Beller, and Thomas H. Riermeier). / 2.11:
Catalytic Enantioselective Alkylation of Alkenes by Chiral Metallocenes (Amir H. Hoveyda). / 2.12:
Palladium-Catalyzed Olefinations of Aryl Halides (Heck Reaction) and Related Transformations (Matthias Beller, Alexander Zapf, and Thomas H. Riermeier). / 2.13:
Palladium-Catalyzed Allylic Substitutions (Andreas Heumann). / 2.14:
Alkene and Alkyne Metathesis in Organic Synthesis (Oliver R. Thiel). / 2.15:
Homometallic Lanthanoids in Synthesis: Lanthanide Triflate-catalyzed Synthetic Reactions (Sh&umarc; Kobayashi). / 2.16:
Lanthanide Complexes in Asymmetric Two-Center Catalysis (Masakatsu Shibasaki, Hiroaki Sasai, and Naoki Yoshikawa). / 2.17:
Bismuth Reagents and Catalysts in Organic Synthesis (Axel Jacobi von Wangelin). / 2.18:
Transition Metal-Mediated Reactions. / 3:
Fischer-Type Carbene Complexes (Karl Heinz Dotz and Ana Minatti). / 3.1:
Titanium-Carbene Mediated Reactions (Nicos A. Petasis). / 3.2:
The McMurry Reaction and Related Transformations (Alois Furstner). / 3.3:
Chromium(II)-Mediated and -Catalyzed C-C Coupling Reactions (David M. Hodgson and Paul J. Comina). / 3.4:
Manganese(III)-Based Oxidative Free-Radical Cyclizations (Barry B. Snider). / 3.5:
Titanium-Mediated Reactions (Rudolf O. Duthaler, Frank Bienewald, and Andreas Hafner). / 3.6:
Zinc-Mediated Reactions (Axel Jacobi von Wangelin and Mathias U. Frederiksen). / 3.7:
The Conjugate Addition Reaction (A. Alexakis). / 3.8:
Carbometalation Reactions of Zinc Enolate Derivatives (Daniella Banon-Tenne and Ilan Marek). / 3.9:
Iron Acyl Complexes (Karola Ruck-Braun). / 3.10:
Iron-Diene Complexes (Hans-Joachim Knolker). / 3.11:
Chromium-Arene Complexes (Hans-Gunther Schmalz and Florian Dehmel). / 3.12:
Pauson-Khand Reactions (D. Strubing and M. Beller). / 3.13:
Subject Index.
Preface.
General. / 1:
Basic Aspects of Organic Synthesis with Transition Metals (Barry M. Trost). / 1.1:
10.

図書

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