Boronic esters as protective groups in carbohydrate chemistry: processes for acylation, silylation and alkylation of glycoside-derived boronates-Reference-Cited by-同舟云学术

Boronic esters as protective groups in carbohydrate chemistry: processes for acylation, silylation and alkylation of glycoside-derived boronates

Published:2017 Issue:1 Volume:15 Page:132-143
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Mancini Ross S.¹²³⁴,Lee Jessica B.¹²³⁴,Taylor Mark S.¹²³⁴

Affiliation:

1. Department of Chemistry

2. University of Toronto

3. Toronto

4. Canada

Abstract

Boronic esters are employed in streamlined protocols for protection, functionalization and deprotection of glycosides, avoiding isolation and purification of intermediates.

Funder

Natural Sciences and Engineering Research Council of Canada

Ministry of Research and Innovation

Canada Foundation for Innovation

The McLean Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2017/OB/C6OB02278B

Reference43 articles.

1. ARENEBORONATES FROM DIOLS AND POLYOLS1

2. 1359. Boric acid derivatives as reagents in carbohydrate chemistry. Part V. The interaction of phenylboronic acid with methyl pentopyranosides: syntheses of 3- and 2,4-substituted ribose derivatives

3. 1360. Boric acid derivatives as reagents in carbohydrate chemistry. Part VI. Phenylboronic acid as a protecting group in disaccharide synthesis

4. 156. Boric acid derivatives as reagents in carbohydrate chemistry. Part III. The interaction of phenylboronic acid with methyl xylofuranosides and the isolation of the four methyl xylosides

5. 450. The interaction of phenylboronic acid with hexosides

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