Organic syntheses based on name reactions and unnamed reactions
著者
書誌事項
Organic syntheses based on name reactions and unnamed reactions
（Tetrahedron organic chemistry series, v. 11）
Pergamon Press, c1994
- : hardcover
- : flexicover
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注記
Includes index
内容説明・目次
- 巻冊次
-
: flexicover ISBN 9780080402796
内容説明
Synthetically useful organic reactions or reagents are often referred to by the name of the discoverer(s) or developer(s). Older name reactions are described in text books, but more recently developed synthetically useful reactions that may have been associated occasionally with a name are not always well known. For neither of the above are experimental procedures or references easy to find.In this monograph approximately 500 name reactions are included, of which over 200 represent newer name reactions and modern reagents. Each of these reactions are extremely useful for the contemporary organic chemistry researcher in industry or academic institutions. This book provides the information in an easily accessible form.In addition to seminal references and reviews, one or more examples for each name reaction are provided and a complete typical experimental procedure is included, to enable the student or researcher to immediately evaluate reaction conditions.Besides an alphabetical listing of reactions and reagents, cross references permit the organic practitioner to find those name reactions or reagents that enable specific transformations, such as, conversion of amines to nitriles, stereoselective reduction, fluoroalkylation, phenol alkynylation, asymmetric syntheses, allylic alkylation, nucleoside synthesis, cyclopentanation, hydrozirconation, to name a few. Emphasis has been placed on stereoselective and regioselective transformations as well as on enantioselective processes. The listing of reactions and reagents is supported by four indexes.
目次
Contains approximately 500 reactions listed alphabetically, of which a selection follows:
Alder: (Ene) Reaction. Baer - Fischer: Amino Sugar Synthesis. Barton: Deamination. Chan: Reduction of Acetylenes. Collman: Carbonylation Reagent. Dakin: Oxidation. Danheiser: Annulation. Ehrlich - Sachs: Aldehyde Synthesis. Evans: Chiral Auxiliary. Ferrier: Carbohydrate Synthesis. Fujiwara - Heck: Coupling. Gassman: Oxindole Synthesis. Haddadin - Issidorides: Quinoxaline Synthesis. Henbest: Iridium Reagent. Hoffman - Yamamoto: Stereoselctive Allylation. Isay: Pteridine Synthesis. Kabe: Chromanone Synthesis. Krief - Reich: Olefination. Lehn: Cryptand Synthesis. Leuckart - Wallace: Reductive Amination. McFadyen - Stevens: Ester Reduction. Nazarov: Cyclopentenone Synthesis. Olofson: Reagent. Pfitzinger: Quinoline Synthesis. Regitz: Diazo Transfer. Sakurai: Allylation. Scholtz: Indolizine Synthesis. Sharpless: Asymmetric Dihydroxylation. Stork: Reductive Cyclization. Suzuki: Vinyl Coupling. Tebbe: Olefination. Tsuji - Trost: Allylation. Ullmann - Fedvadjan: Acridine Synthesis. Van Boom: Phosphorylating Reagent. Vilsmeier - Haack - Viehe Reagent. Wacker - Tsuji: Olefin Oxidation. Wissner: Hydroxy Ketone Synthesis. Wolff: Rearrangement. Yamazaki: Cyanoaniline Synthesis. Zinke - Ziegler: Synthesis of Calixarenes. Names Index. Reagents Index. Reactions Index. Functional Group Transformations Index.
- 巻冊次
-
: hardcover ISBN 9780080402802
内容説明
Synthetically useful organic reactions or reagents are often referred to by the name of the discoverer(s) or developer(s). "Older name reactions" are described in text books, but more recently developed synthetically useful reactions that may have been associated occasionally with a name are not always well known. For neither of the above are experimental procedures or references easy to find. In this monograph approximately 500 name reactions are included, of which over 200 represent newer name reactions and modern reagents. Each of these reactions are extremely useful for the contemporary organic chemistry researcher in industry or academic institutions. This book provides the information in an easily accessible form. In addition to seminal references and reviews, one or more examples for each name reaction are provided and a complete typical experimental procedure is included, to enable the student or researcher to immediately evaluate reaction conditions.
Besides an alphabetical listing of reactions and reagents, cross references permit the organic practitioner to find those name reactions or reagents that enable specific transformations, such as, conversion of amines to nitriles, stereoselective reduction, fluoroalkylation, phenol alkynylation, asymmetric syntheses, allylic alkylation, nucleoside synthesis, cyclopentanation, hydrozirconation, to name a few. Emphasis has been placed on stereoselective and regioselective transformations as well as on enantioselective processes. The listing of reactions and reagents is supported by four indexes, of which one is a pull-out table of functional group transformations.
目次
- Alder (ene) reaction
- Auwers - flavone synthesis
- Baer-Fischer - amino sugar synthesis
- Chan - reduction of acetylenes
- Collman - carbonylation reagent
- Dakin - oxidation
- Ehrlich-Sachs - aldehyde synthesis
- Ferrier - carbohydrate synthesis
- Friedel-Crafts - alkylation-acylation
- Gassman - oxindole synthesis
- Haddadin-Issidorides - quinoxaline synthesis
- Henbest - iridium reagent
- Isay - pteridine synthesis
- Kabe - chromanone synthesis
- Leuckart-Wallace - reductive amination
- McFadyen-Stevens - ester reduction
- Michael addition
- Nazarov - cyclopentenone synthesis
- Olofson - reagent
- Paal-Knorr - pyrrole synthesis
- Pfitzinger - quinoline synthesis
- Regitz - diazo transfer
- Sakurai - allylation
- Scholtz - indolizine synthesis
- Suzuki - vinyl coupling
- Tebbe - olefination
- Ullmann-Fedvadjan - acridine synthesis
- Van Boom - phosphorylating reagent
- Vilsmeier-Haack-Viehe reagent
- Wacker-Tsuji - olefin oxidation
- Wissner - hydroxy ketone synthesis
- Wolff rearrangement
- Yamazaki - cyanoaniline synthesis
- Zinke-Ziegler - synthesis of calixarenes
- name index
- reagent index
- index to type of reactions
- index to the synthesis of functional groups. (Part Contents).
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