Selective substitution at the 3-position in a 3,4-O-dibutylstannylene-d-galactopyranose derivative. An improved synthesis of 2,4,6-tri-O-benzyl-d-galactose-Reference-Cited by-同舟云学术

Selective substitution at the 3-position in a 3,4-O-dibutylstannylene-d-galactopyranose derivative. An improved synthesis of 2,4,6-tri-O-benzyl-d-galactose

Published:1977-07 Issue:2 Volume:56 Page:419-422
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Nashed Mina A.,Anderson Laurens

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference10 articles.

1. O-benzylated thio sugars: 2,3,4- and 2,4,6-tri-O-benzyl-1-thio-β-d-galactopyranose

2. Organotin derivatives and the selective acylation and alkylation of the equatorial hydroxy group in a vicinal, equatorial-axial pair

3. Preparation and Synthetic Utility of Some Organotin Derivatives of nucleosides

4. Complete regiospecificity in the benzylation of a cis-diol by the stannylidene procedure

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