Issue 24, 2017
From the journal:

Green Chemistry

Base-mediated tandem sulfonylation and oximation of alkenes in water†

Bin Wang,ab   Lin Tang,a   Liyan Liu,a   Yanan Li,a   Yu Yanga  and  Zhiyong Wang ORCID logo *a  

* Corresponding authors

a Hefei National Laboratory for Physical Sciences at Microscale, CAS Key Laboratory of Soft Matter Chemistry and Department of Chemistry & Collaborative Innovation Center of Suzhou Nano Science and Technology, University of Science and Technology of China, Hefei, P. R. China

b Key Laboratory of Xin'an Medicine, Ministry of Education, Anhui University of Chinese Medicine, Hefei, P. R. China
E-mail: zwang3@ustc.edu.cn
Fax: (+86) 551-6360-3185

Abstract

A base-mediated bifunctionalization of alkenes for the synthesis of α-sulfonylethanone oximes was developed in water under metal-free conditions. This reaction features a wide substrate scope and facile starting materials to afford the desired products in high yields.

Graphical abstract: Base-mediated tandem sulfonylation and oximation of alkenes in water

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Supplementary files

Article information

DOI
https://doi.org/10.1039/C7GC03051G
Article type
Communication
Submitted
10 Oct 2017
Accepted
15 Nov 2017
First published
16 Nov 2017

Green Chem., 2017,19, 5794-5799

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Base-mediated tandem sulfonylation and oximation of alkenes in water

B. Wang, L. Tang, L. Liu, Y. Li, Y. Yang and Z. Wang, Green Chem., 2017, 19, 5794 DOI: 10.1039/C7GC03051G

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