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Reactions and syntheses in the organic chemistry laboratory

Author: Lutz-Friedjan Tietze
Publisher: Weinheim : Wiley-VCH, 2007.
Edition/Format:   Print book : Government publication : EnglishView all editions and formats
Summary:

Presenting a broad spectrum of modern total synthesis of natural products, pharmaceuticals, heterocycles, C-C bonding and biochemical reactions, this practical textbook readily guides readers to the  Read more...

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Genre/Form: Laboratory manuals
Material Type: Government publication, Internet resource
Document Type: Book, Internet Resource
All Authors / Contributors: Lutz-Friedjan Tietze
ISBN: 9783527312238 3527312234
OCLC Number: 259976523
Notes: Revised edition of: Reactions and syntheses in the organic chemistry laboratory / Lutz-Friedjan Tietze, Theophil Eicher ; with the assistance of G.V. Kiedrowski [and others] ; translated from the German by Dagmar Ringe. c1989.
Description: xvi, 582 pages : illustrations ; 28 cm
Contents: C-C BOND FORMATION Nucleophilic Addition to Aldehydes, Ketones, Carboxylic Acid Derivatives (Esters, Anhydrides) and Alpha,Beta-unsaturated Carbonyl Compounds; Carbonyl Olefination Alkylation of Aldehydes/ Ketones, Carboxylic Acids and Beta-dicarbonyl Compounds Reactions of the Aldol and Mannich Type Electrophilic and Nucleophilic Acylation Reactions of Alkenes via Carbenium Ions Transition-metal Mediated Reactions Pericyclic Reactions Radical Reactions OXIDATION AND REDUCTION Epoxidation of C=C Bonds Dihydroxylation of C=C Bonds Oxidation of Alcohols to Carbonyl Compounds Enantioselective Reduction of Ketones HETEROCYCLIC COMPOUNDS Three- and Four-membered Heterocycle Five-membered Heterocycles Six-membered Heterocycles Condensed Heterocycles Other Heterocyclic Systems, Heterocyclic Dyes SELECTED NATURAL PRODUCTS Amino Acids and Peptides Alkaloids Terpenoids, Steroids Carbohydrates
Responsibility: Lutz F. Tietze [and others].
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"I thoroughly recommend this textbook for any of its target audience. It should be in every library ? And on the personal bookshelves of each of its intended readers as well? An invaluable aid." - Read more...

 
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