Cycloaddition Reactions in Carbohydrate Chemistry
Published on 1. January 1992
Book
Hardback
182 pages
978-0-8412-2429-2 (ISBN)
Description
Provides discussions on recent advances in the cycloaddition chemistry of carbohydrates, including inter- and intramolecular Diels-Alder reactions, dipolar addition reactions, and the use of carbohydrate-derived chiral auxiliaries. Includes applications to the synthesis of natural products and examines the stereochemical aspects of cycloaddition processes. Emphasizes the use of carbohydrate-derived substrates in cycloaddition reactions. Valuable reading for anyone
interested in the synthetic organic chemistry of carbohydrates.
interested in the synthetic organic chemistry of carbohydrates.
More details
Series
Language
English
Place of publication
Washington
United States
Target group
Professional and scholarly
Dimensions
Height: 235 mm
Width: 157 mm
Thickness: 18 mm
Weight
411 gr
ISBN-13
978-0-8412-2429-2 (9780841224292)
Copyright in bibliographic data is held by Nielsen Book Services Limited or its licensors: all rights reserved.
Schweitzer Classification
Person
Content
Cycloaddition Reactions in Carbohydrate Chemistry: An Overview ; Carbohydrate Dienophiles in [4 + 2] Cycloadditions ; Pyranose-Derived Dienes and Conjugated Enals: Preparation and Diels-Alder Cycloaddition Reactions ; Synthesis of *b-Lactams from Unsaturated Sugars and Isocyanates ; Diels-Alder Cycloaddition to Unsaturated Sugars: Stereocontrol as a Function of Structure and Stereochemistry ; The [4 + 2] Cycloaddition of Azodicarboxylates and Cyclic Vinyl Ethers: Application to the Synthesis of Simple and Complex 2-Aminosaccharides ; Glycosylmanganese Pentacarbonyl Complexes: An Organomanganese-Based Approach to the Synthesis of C-Glycosyl Derivatives ; Inter- and Intramolecular Diels-Alder Reactions of Sugar Derivatives ; Carbohydrates as Chiral Templates in Stereoselective [4 + 2] Cycloaddition Reactions ; Aqueous Cycloadditions Using Glycoorganic Substrates: Stereo- and Physicochemical Aspects ; Stereoselectivity of 1,3-Dipolar Cycloaddition of Clycosyl Nitrones to N-Arylmaleimides