Photo-induced radical transformations of tosyl cyanide
Author:
Affiliation:
1. Green Catalysis Centre, College of Chemistry, Zhengzhou University, Zhengzhou 450001, China
2. School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, Singapore 637459, Singapore
Abstract
Funder
National Natural Science Foundation of China
Zhengzhou University
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2024/OB/D3OB01771K
Reference65 articles.
1. Toluenesulfonyl Cyanide (TsCN)
2. Non-toxic cyanide sources and cyanating agents
3. G. J.Griffiths and J. T.Markiewicz , in Encyclopedia of Reagents for Organic Synthesis , 2014 , pp. 1–5
4. A Click Chemistry Approach to Tetrazoles by Huisgen 1,3-Dipolar Cycloaddition: Synthesis of 5-Sulfonyl Tetrazoles from Azides and Sulfonyl Cyanides We thank the National Institute of General Medical Sciences, National Institutes of Health (GM-28384), the National Science Foundation (CHE-9985553), the Skaggs Institute for Chemical Biology for a Predoctoral Fellowship (Z.D.), and the W. M. Keck Foundation for financial support. Dedicated to Professor Rolf Huisgen, the pioneer of this large and extremely useful family of reactions.
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