Direct N-glycosylation of tosyl and nosyl carbamates with trichloroacetimidate donors-Reference-Cited by-同舟云学术

Direct N-glycosylation of tosyl and nosyl carbamates with trichloroacetimidate donors

Published:2021 Issue:34 Volume:45 Page:15386-15391
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Khanam Ariza¹,Mandal Pintu Kumar¹²^ORCID

Affiliation:

1. Medicinal & Process Chemistry Division, CSIR-Central Drug Research Institute, BS-10/1, Sector 10, Jankipuram extn, Sitapur Road, P.O. Box 173, Lucknow 226031, India

2. Academy of Scientific and Innovative Research, Ghaziabad-201002, India

Abstract

Acidic sulphonamide reactants act as both catalysts and nucleophiles to afford the desired N-glycofuranosyl sulfonamides stereoselectively.

Funder

Science and Engineering Research Board

Central Drug Research Institute

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2021/NJ/D1NJ02051J

Reference60 articles.

1. Exploring the Effect of Bioisosteric Replacement of Carboxamide by a Sulfonamide Moiety on N-Glycosidic Torsions and Molecular Assembly: Synthesis and X-ray Crystallographic Investigation of N-(β-D-Glycosyl)sulfonamides as N-Glycoprotein Linkage Region An

2. Unexpected furanose/pyranose equilibration of N-glycosyl sulfonamides, sulfamides and sulfamates

3. Ferrier sulfamidoglycosylation of glycals catalyzed by nitrosonium tetrafluoroborate: Towards new carbonic anhydrase glycoinhibitors

4. A Prodrug Approach Toward Cancer-Related Carbonic Anhydrase Inhibition

5. Synthesis and carbonic anhydrase inhibitory effects of new N-glycosylsulfonamides incorporating the phenol moiety

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