
Cycloaddition Reactions in Organic Synthesis
Wiley-VCH (Publisher)
1st Edition
Published on 15. January 2002
Book
Hardback
XII, 332 pages
978-3-527-30159-1 (ISBN)
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Description
Cycloaddition reactions are among the most important tools for synthesis in organic chemistry, since these reactions are vital to the modern synthesis of natural products and biologically active substances.
Metal catalysis plays an increasingly important role in these reactions, often allowing several stereocenters to be selectively created and integrated in the target molecules. Kobayashi and Jorgensen's handbook provides numerous examples of metal-catalyzed reactions, including [2+1], [3+2] and [4+2] cycloadditions. Important reactions such as carbo- and hetero-Diels-Alder, carbocyclic, cyclopropanation and 1,3-dipolar cycloaddition reactions are discussed. A large number of experimental procedures gives a concrete idea of the use of metal-catalyzed cycloaddition reactions in modern synthesis.
The book is aimed at chemists in industry or academia, who want to effectively use cycloadditions in their work.
Reviews / Votes
"This book should find its way into most good chemistry libraries."Chemistry & IndustryMore details
Edition
1., Auflage
Language
English
Place of publication
Weinheim
Germany
Target group
College/higher education
Professional and scholarly
Organiker, Naturstoffchemiker, Pharmazeutische Chemiker, Medizinische Chemiker, Chemiker in der Industrie
Illustrations
338
279 s/w Abbildungen, 59 s/w Tabellen
Ill.
Dimensions
Height: 24 cm
Width: 17 cm
Thickness: 20 mm
Weight
795 gr
ISBN-13
978-3-527-30159-1 (9783527301591)
Schweitzer Classification
Content
Introduction
Catalytic Asymmetric Diels-Alder Reactions
Recent Advances in Palladium-catalyzed Cycloadditions Involving Trimethylenemethane and its Analogs
Enantioselective [2+1] Cycloaddition: Cyclopropanation with Zinc Carbenoids
Catalytic Enantioselective Cycloaddition Reactions of Carbonyl Compounds
Catalytic Enantioselective Aza Diels-Alder Reactions
Asymmetric Metal-catalyzed 1,3-Dipolar Cycloaddition Reactions
Aqua Complex Lewis Acid Catalysts for Asymmetric 3+2 Cycloaddition Reactions
Theoretical Calculations of Metal-catalyzed Cycloaddition Reactions
Index