Stereochemical features of the [1,2]-Wittig rearrangement of O-glycosides derived from D-galactono- and D-xylono-γ-lactones: A new approach to the core part of zaragozic acids-Reference-Cited by-同舟云学术

Stereochemical features of the [1,2]-Wittig rearrangement of O-glycosides derived from D-galactono- and D-xylono-γ-lactones: A new approach to the core part of zaragozic acids

Published:1999-03 Issue:10 Volume:40 Page:1917-1920
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Tomooka Katsuhiko,Kikuchi Makoto,Igawa Kazunobu,Keong Ping-Huai,Nakai Takeshi

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference13 articles.

1. (1,2)-Wittig Rearrangement: Stereochemical Features and Synthetic Utilities.

2. Recent Developments in the [1,2]-Wittig Rearrangement

3. [1,2]-Wittig Rearrangement of Acetal Systems: A Highly Stereocontrolled Conversion of O-Glycosides to C-Glycosides

4. The Chemistry of C-Glycosides;Levy,1995

5. Recent advances in stereoselective c-glycoside synthesis

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