Chemistry of 1-Alkoxy-1-glycosyl Radicals: Formation of β-Mannopyranosides by Radical Decarboxylation and Decarbonylation of manno-Heptulosonic Acid Glycoside Derivatives-Reference-Cited by-同舟云学术

Chemistry of 1-Alkoxy-1-glycosyl Radicals: Formation of β-Mannopyranosides by Radical Decarboxylation and Decarbonylation of manno-Heptulosonic Acid Glycoside Derivatives

Published:1996-01-01 Issue:18 Volume:61 Page:6189-6198
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Crich David¹,Hwang Jae-Taeg¹,Yuan Hongwei¹

Affiliation:

1. Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, Illinois 60607-7061

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo960799q

Reference68 articles.

1. Stereoselective Synthesis of β-Mannopyranosides via the Temporary Silicon Connection Method

2. Concise synthesis of a taxol A-ring synthon: Formation of a 1,2-alkylidene linkage via acetylene chemistry

3. Chemistry of 1-Alkoxy-1-glycosyl Radicals: The Manno- and Rhamnopyranosyl Series. Inversion of α- to β-Pyranosides and the Fragmentation of Anomeric Radicals

4. A Convergent and Stereocontrolled Synthetic Route to the Core Pentasaccharide Structure of Asparagine-Linked Glycoproteins

5. Synthesis of β-mannopyranosides from α-epimers by radical inversion

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