Synthesis, conformation, and glycosidic coupling reactions of highly active substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-α-d-xylopyranose-Reference-Cited by-同舟云学术

Synthesis, conformation, and glycosidic coupling reactions of highly active substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-α-d-xylopyranose

Published:1994-05 Issue: Volume:258 Page:49-58
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Yang Guangbin,Kong Fanzuo,Fraser Robert R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference20 articles.

1. Synthesis of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4,6-tri-O-benzyl- and 1,2-anhydro-3,4,6-tri-O-(p-bromobenzyl)-α-d-galactopyranose

2. Synthesis, conformational analysis, and the glycosidic coupling reaction of substituted 2,7-dioxabicyclo[4.1.0]heptanes: 1,2-anhydro-3,4-di-O-benzyl-β-l- and β-d-rhamnopyranoses

3. Synthesis and Conformational Analysis of 1, 2-Anhydro-3, 4-di-O-benzyl-6-deoxy-α-D-glucopyranose

4. Synthesis and conformation of 1,2-anhydro,3,4-6-tri-O-benzyl-β-d-talopyranose

5. Z. Gan and F. Kong, unpublished results.

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