Issue 63, 2015
From the journal:

RSC Advances

A convenient access to β-iodo sulfone by the iodine-mediated iodosulfonylation of alkenes†

Kai Sun,*a   Yunhe Lv,a   Zhonghong Zhu,a   Yongqing Jiang,a   Jiejie Qi,a   Hankui Wu,a   Zhiguo Zhang,b   Guisheng Zhangb  and  Xin Wang*a  

* Corresponding authors

a College of Chemistry and Chemical Engineering, Anyang Normal University, Anyang, Henan 455000, P. R. China
E-mail: sunk468@nenu.edu.cn, wangx933@nenu.edu.cn

b College of Chemistry and Chemical Engineering, Henan normal university, Xinxiang, Henan 453007, P. R. China

Abstract

A novel iodine-mediated intermolecular iodosulfonylation reaction of alkenes for dual C–S and C–I bond formation is described. A series of alkenes could be selectively converted into the corresponding β-iodo sulfones, which are versatile building blocks in organic synthesis and medicinal chemistry. Molecular iodine was the iodine source in this reaction.

Graphical abstract: A convenient access to β-iodo sulfone by the iodine-mediated iodosulfonylation of alkenes

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Article information

DOI
https://doi.org/10.1039/C5RA07065A
Article type
Communication
Submitted
19 Apr 2015
Accepted
22 May 2015
First published
22 May 2015

RSC Adv., 2015,5, 50701-50704

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A convenient access to β-iodo sulfone by the iodine-mediated iodosulfonylation of alkenes

K. Sun, Y. Lv, Z. Zhu, Y. Jiang, J. Qi, H. Wu, Z. Zhang, G. Zhang and X. Wang, RSC Adv., 2015, 5, 50701 DOI: 10.1039/C5RA07065A

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