Issue 32, 2021

Nickel-catalyzed Heck reaction of cycloalkenes using aryl sulfonates and pivalates

Abstract

Nickel-catalyzed Heck reaction of cycloalkenes delivers unusual conjugated arylated isomers. Nickel(0) catalysts ligated by chelating dialkylphosphines effectively activate not only aryl triflates as electrophiles, but also less reactive aryl mesylates, tosylates and pivalates. The omission of bases allows nickel hydride species to exist long enough to perform in situ olefin isomerization of initial Heck adducts.

Graphical abstract: Nickel-catalyzed Heck reaction of cycloalkenes using aryl sulfonates and pivalates

Supplementary files

Article information

Article type
Communication
Submitted
03 Feb 2021
Accepted
12 Mar 2021
First published
12 Mar 2021

Chem. Commun., 2021,57, 3933-3936

Nickel-catalyzed Heck reaction of cycloalkenes using aryl sulfonates and pivalates

J. S. Zhou, X. Huang, S. Teng and Y. R. Chi, Chem. Commun., 2021, 57, 3933 DOI: 10.1039/D1CC00634G

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