Issue 14, 2021

Regioselective synthesis of indenones via nickel-catalyzed Larock annulations

Abstract

We present herein highly effective nickel-catalyzed Larock annulations of substituted 2-formylphenyl trifluoromethanesulfonate with alkynes to provide an access to a wide range of indenones that are valuable synthetic intermediates for natural compounds. This catalytic system is shown to proceed through a redox neutral arylation to produce indenone products in high yields with excellent regioselectivities. In addition, a highly efficient transformation of the natural product estrone via Ni-catalyzed Larock annulation can also be achieved.

Graphical abstract: Regioselective synthesis of indenones via nickel-catalyzed Larock annulations

Supplementary files

Article information

Article type
Research Article
Submitted
30 Mar 2021
Accepted
12 May 2021
First published
13 May 2021

Org. Chem. Front., 2021,8, 3847-3852

Regioselective synthesis of indenones via nickel-catalyzed Larock annulations

F. Liu, Y. Li, X. Wang, Q. Qiang, Z. Yan, Y. Zhang and Z. Rong, Org. Chem. Front., 2021, 8, 3847 DOI: 10.1039/D1QO00487E

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