Issue 3, 2014

Ru(ii)-catalyzed rearrangement of the allenic sulfide bearing propargyl moiety: efficient formation of benzene derivatives

Abstract

[RuCl2(p-cymene)]2 efficiently catalyzes the rearrangement of allenic sulfides bearing the propargyl moiety to afford 1,2,4-trisubstituted benzene derivatives. The alkyne-Ru(II) carbene [2 + 2] cycloaddition/ring opening process has been proposed in the reaction mechanism.

Graphical abstract: Ru(ii)-catalyzed rearrangement of the allenic sulfide bearing propargyl moiety: efficient formation of benzene derivatives

Supplementary files

Article information

Article type
Research Article
Submitted
02 Jan 2014
Accepted
21 Jan 2014
First published
07 Feb 2014

Org. Chem. Front., 2014,1, 235-239

Author version available

Ru(II)-catalyzed rearrangement of the allenic sulfide bearing propargyl moiety: efficient formation of benzene derivatives

L. Peng, X. Zhang, J. Ma and J. Wang, Org. Chem. Front., 2014, 1, 235 DOI: 10.1039/C4QO00001C

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