Stereoselective oxidative <i>O</i>-glycosylation of disarmed glycosyl iodides with alcohols using PIDA as the promoter-Reference-Cited by-同舟云学术

Stereoselective oxidative O-glycosylation of disarmed glycosyl iodides with alcohols using PIDA as the promoter

Published:2023 Issue:32 Volume:21 Page:6479-6483
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Boulogeorgou Maria A.¹,Toskas Alexandros¹,Gallos John K.¹^ORCID,Stathakis Christos I.¹^ORCID

Affiliation:

1. Department of Chemistry, Aristotle University of Thessaloniki, Thessaloniki 54124, Greece

Abstract

“Disarmed” glycosyl iodides as glycosyl donors in PIDA promoted stereoselective O-glycosylations. An extremely mild alternative to existing methodologies.

Funder

European Social Fund

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D3OB00929G

Reference33 articles.

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2. H. J.Gabius , The Sugar Code: Fundamentals of Glycosciences , Wiley-Blackwell , Weinheim, Germany , 2009

3. Glycosylation and the Immune System

4. Chemical glycosylation in the synthesis of glycoconjugate antitumour vaccines

5. Amygdalin: Toxicity, Anticancer Activity and Analytical Procedures for Its Determination in Plant Seeds

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