Protecting-group-free S-glycosylation towards thioglycosides and thioglycopeptides in water-Reference-Cited by-同舟云学术

Protecting-group-free S-glycosylation towards thioglycosides and thioglycopeptides in water

Published:2021 Issue:8 Volume:23 Page:2907-2912
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Zhang Gao-Lan¹²³⁴,Gadi Madhusudhan Reddy¹²³⁴^ORCID,Cui Xikai¹²³⁴,Liu Ding¹²³⁴,Zhang Jiabin¹²³⁴,Saikam Varma¹²³⁴^ORCID,Gibbons Christopher¹²³⁴,Wang Peng G.¹²³⁴,Li Lei¹²³⁴^ORCID

Affiliation:

1. Department of Chemistry

2. Georgia State University

3. Atlanta

4. USA

Abstract

A facile and green S-glycosylation method is developed, in which Ca(OH)₂ promoted the coupling of protection-group-free fluoride donors and thiol acceptors in water, affording various thioglycosides and thioglycopeptides.

Funder

National Institute of General Medical Sciences

National Heart, Lung, and Blood Institute

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/GC/D1GC00098E

Reference56 articles.

1. 1,2-cis Alkyl glycosides: straightforward glycosylation from unprotected 1-thioglycosyl donors

2. En Route to the Transformation of Glycoscience: A Chemist’s Perspective on Internal and External Crossroads in Glycochemistry