Issue 89, 2021

Pd-catalyzed allylative dearomatisation using Grignard reagents

Abstract

Pd-catalyzed allylative dearomatisation of naphthyl halides is shown to be feasible by employing Grignard reagents. The high reactivity of the nucleophile allows for fast reactions and low catalyst loading, while a plethora of successfully substituted compounds illustrate the broad scope. Five membered heteroaromatic compounds are also demonstrated to be reactive under similar conditions.

Graphical abstract: Pd-catalyzed allylative dearomatisation using Grignard reagents

Supplementary files

Article information

Article type
Communication
Submitted
04 Oct 2021
Accepted
15 Oct 2021
First published
25 Oct 2021
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2021,57, 11807-11810

Pd-catalyzed allylative dearomatisation using Grignard reagents

C. Boldrini and S. R. Harutyunyan, Chem. Commun., 2021, 57, 11807 DOI: 10.1039/D1CC05609C

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