Issue 51, 2021

Alkoxysulfenylation of alkenes: development and recent advances

Abstract

Among the wide variety of synthetic transformations of inexpensive and abundant feedstock alkenes, vicinal difunctionalization of carbon–carbon double bonds represent one of the most powerful and effective strategies for the introduction of two distinct functional groups into target compounds in a one-pot process. In this context, the direct alkoxysulfenylation of alkenes has emerged as an elegant method to construct valuable β-alkoxy sulfides in an atom- and pot-economic manner utilizing readily accessible starting materials. Here, we review the available literature on this appealing research topic by hoping that it will be beneficial for eliciting further research and thinking in this domain.

Graphical abstract: Alkoxysulfenylation of alkenes: development and recent advances

Article information

Article type
Review Article
Submitted
22 mei 2021
Accepted
24 aug 2021
First published
01 okt 2021
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2021,11, 32513-32525

Alkoxysulfenylation of alkenes: development and recent advances

Y. Cao, S. Soleimani-Amiri, R. Ahmadi, A. Issakhov, A. G. Ebadi and E. Vessally, RSC Adv., 2021, 11, 32513 DOI: 10.1039/D1RA03980F

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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