Issue 51, 2021

Ru(ii)-catalyzed allenylation and sequential annulation of N-tosylbenzamides with propargyl alcohols

Abstract

We hereby report Ru(II)-catalyzed C(sp2)–H allenylation of N-tosylbenzamides to access multi-substituted allenylamides. Furthermore, the allenylamides were converted to the corresponding isoquinolone derivatives via base mediated annulation. The current protocol features low catalyst loading, mild reaction conditions, high functional group compatibility and desired scalability. The unique functionality of the afforded allenes allowed further transformations to expand the practicality of the protocol.

Graphical abstract: Ru(ii)-catalyzed allenylation and sequential annulation of N-tosylbenzamides with propargyl alcohols

Supplementary files

Article information

Article type
Communication
Submitted
02 Apr 2021
Accepted
25 May 2021
First published
25 May 2021

Chem. Commun., 2021,57, 6280-6283

Ru(II)-catalyzed allenylation and sequential annulation of N-tosylbenzamides with propargyl alcohols

S. Kumar, A. M. Nair and C. M. R. Volla, Chem. Commun., 2021, 57, 6280 DOI: 10.1039/D1CC01768C

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