The reaction of 2-hydroxyglycal esters with alcohols in the presence of N-iodosuccinimide, stereoselective synthesis of α anomers of alkyl 3-deoxyhex-2-enopyranosides and 3,4-dideoxyhex-3-enopyranosid-2-uloses-Reference-Cited by-同舟云学术

The reaction of 2-hydroxyglycal esters with alcohols in the presence of N-iodosuccinimide, stereoselective synthesis of α anomers of alkyl 3-deoxyhex-2-enopyranosides and 3,4-dideoxyhex-3-enopyranosid-2-uloses

Published:1987-09 Issue: Volume:167 Page:187-196
ISSN:0008-6215
Container-title:Carbohydrate Research
language:en
Short-container-title:Carbohydrate Research

Author:

Varela Oscar,de Fina Griselda M.,de Lederkremer Rosa M.

Publisher

Elsevier BV

Subject

Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry

Reference37 articles.

1. New route for the synthesis of 3-deoxyaldos-2-uloses

2. Some progeny of 2,3-unsaturated sugars - they little resemble grandfather glucose: ten years later

3. Progeny of 2,3-unsaturated sugars. They little resemble Grandfather Glucose

4. Sugar enolones: synthesis, reactions of preparative interest, and γ-pyrone formation

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