“Armed-disarmed” glycosidation strategy based on glycosyl donors and acceptors carrying phosphoroamidate as a leaving group: A convergent synthesis of globotriaosylceramide-Reference-Cited by-同舟云学术

“Armed-disarmed” glycosidation strategy based on glycosyl donors and acceptors carrying phosphoroamidate as a leaving group: A convergent synthesis of globotriaosylceramide

Published:1997-12 Issue:52 Volume:38 Page:8969-8972
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hashimoto Shun-ichi,Sakamoto Hiroki,Honda Takeshi,Abe Hiroshi,Nakamura Sei-ichi,Ikegami Shiro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference46 articles.

1. Armed and disarmed n-pentenyl glycosides in saccharide couplings leading to oligosaccharides

2. n-Pentenyl Glycosides in Organic Chemistry: A Contemporary Example of Serendipity

3. Recent progress in O-glycosylation methods and its application to natural products synthesis

4. Strategies in Oligosaccharide Synthesis

5. “Active” and “latent” thioglycosyl donors in oligosaccharide synthesis. Application to the synthesis of α-sialosides

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