Efficient and stereoselective 1,2-cis glycoside formation of 5-thioaldopyranoses: glycosylation with peracetylated 5-thio-D- arabinopyranosyl and 5-thio-L-fucopyranosyl trichloroacetimidates-Reference-Cited by-同舟云学术

Efficient and stereoselective 1,2-cis glycoside formation of 5-thioaldopyranoses: glycosylation with peracetylated 5-thio-D- arabinopyranosyl and 5-thio-L-fucopyranosyl trichloroacetimidates

Published:1993-07 Issue:31 Volume:34 Page:4949-4952
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Hashimoto Hironobu,Izumi Masayuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Synthesis and enzyme-inhibitory activity of methyl acarviosin analogues having the α- manno configuration

2. Chemie und Biochemie mikrobieller α-Glucosidasen-Inhibitoren

3. Positional isomers of thioxylobiose, their synthesis and inducing ability for d-xylan-degrading enzymes in the yeast cryptococcus albidus

4. Hashimoto, H., Shimada, K., Horito, S. Tetrahedron Lett. (submitted).

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