Issue 8, 2020

Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters

Abstract

Functional group transfer reactions are an important synthetic tool in modern organic synthesis. Herein, we developed a new palladium-catalyzed intermolecular transthioetherification reaction of aryl halides with thioethers and thioesters. The synthetic utility and practicality of this catalytic protocol are demonstrated in a wide range of successful transformations (>70 examples). This catalytic protocol is applicable in carbonylative coupling processes as well, and the first example of carbonylative methylthioesterification of aryl halides has been achieved. Notably, this work also provides an approach to using natural products, such as methionine and selenomethionine, as the functional group sources.

Graphical abstract: Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters

Supplementary files

Article information

Article type
Edge Article
Submitted
01 Nov 2019
Accepted
17 Jan 2020
First published
22 Jan 2020
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY license

Chem. Sci., 2020,11, 2187-2192

Palladium-catalyzed intermolecular transthioetherification of aryl halides with thioethers and thioesters

Y. Li, G. Bao and X. Wu, Chem. Sci., 2020, 11, 2187 DOI: 10.1039/C9SC05532K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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