Peroxodisulfate-assisted synthesis of 2-thiocyanato glycals and their transformation to C-2-thio acrylo/aryl nitrile-substituted glycals-Reference-Cited by-同舟云学术

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Peroxodisulfate-assisted synthesis of 2-thiocyanato glycals and their transformation to C-2-thio acrylo/aryl nitrile-substituted glycals

Published:2024 Issue:62 Volume:60 Page:8071-8074
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Rasool Bisma¹²,Zargar Irshad Ahmad¹²,kundu Sanchari³,Mukherjee Debaraj²³^ORCID

Affiliation:

1. Natural Products and Medicinal Chemistry Division, Indian Institute of Integrative Medicine (CSIR-IIIM), Jammu-180001, India

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

3. Department of Chemical Sciences, Bose Institute Kolkata, EN 80, Sector V, Bidhan Nagar, Kolkata-700091, WB, India

Abstract

An efficient regioselective method to attach thiocyanato groups at the β-position of enol double bonds in sugar enol ethers using KSCN and potassium persulfate has been developed.

Funder

Science and Engineering Research Board

University Grants Commission

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CC/D4CC02201G

Reference26 articles.

1. Synthesis of Branched-Chain Sugars

2. Components of Bacterial Polysaccharides

3. Some Progeny of 2,3-Unsaturated SugarsThey Little Resemble Grandfather Glucose: Twenty Years Later,1

4. Stereochemical problems in macrolide antibiotics

5. Y.Chapleur and F.Chértien , in Preparative Carbohydrate Chemistry , ed. S. Hanessian , Marcel Dekker , New York , 1997 , p. 207

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