Issue 17, 2018

Striving to exploit alkyl electrophiles: challenge and choice in transition metal-catalyzed cross-coupling reactions of sulfones

Abstract

For cross-coupling reactions of alkyl electrophiles, alkyl halides, alkyl tosylates, alkyl acetates and alkyl sulfones exhibit high reaction efficiency when various transition metal catalysts and reaction partners are employed. As crystalline and readily available alkyl electrophiles, alkyl sulfones in radical cross-coupling reactions open a new avenue for modularly generating diverse alkyl compounds. It is believed that more transformations using sulfones as electrophiles will be developed in the near future.

Graphical abstract: Striving to exploit alkyl electrophiles: challenge and choice in transition metal-catalyzed cross-coupling reactions of sulfones

Article information

Article type
Highlight
Submitted
28 Mezh. 2018
Accepted
20 Goue. 2018
First published
23 Goue. 2018

Org. Chem. Front., 2018,5, 2615-2617

Striving to exploit alkyl electrophiles: challenge and choice in transition metal-catalyzed cross-coupling reactions of sulfones

M. Liu, Y. Zheng, G. Qiu and J. Wu, Org. Chem. Front., 2018, 5, 2615 DOI: 10.1039/C8QO00632F

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