Issue 22, 2016
From the journal:

Organic & Biomolecular Chemistry

Three-component oxysulfenylation reaction: two simple and convenient approaches to β-alkoxy sulfides†

Dingyi Wang,a   Rongxing Zhang,a   Wei Ning,a   Zhaohua Yan*a  and  Sen Lin*a  

* Corresponding authors

a College of Chemistry, Nanchang University, Nanchang, Jiangxi 330031, China
E-mail: senlin@ncu.edu.cn, yanzh@ncu.edu.cn

Abstract

An unprecedented method for the synthesis of β-alkoxy sulfides via a NaI/HBr-mediated three-component oxysulfenylation reaction of alkenes with arylsulfinic acids and alcohols is reported. Furthermore, I2-promoted oxysulfenylation of alkenes using sodium arylsulfinates instead of arylsulfinic acids to synthesise various β-alkoxy sulfides is also described.

Graphical abstract: Three-component oxysulfenylation reaction: two simple and convenient approaches to β-alkoxy sulfides

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C6OB00646A
Article type
Paper
Submitted
25 Mar 2016
Accepted
05 May 2016
First published
10 May 2016

Org. Biomol. Chem., 2016,14, 5136-5140

Permissions

Request permissions

Three-component oxysulfenylation reaction: two simple and convenient approaches to β-alkoxy sulfides

D. Wang, R. Zhang, W. Ning, Z. Yan and S. Lin, Org. Biomol. Chem., 2016, 14, 5136 DOI: 10.1039/C6OB00646A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements