Issue 38, 2021

Selective cine-arylation of tert-cyclobutanols with indoles enabled by nickel catalysis

Abstract

In previous literature, tert-cyclobutanols are widely studied for C–C bond activation exclusively leading to the formation of ordinary γ-substituted ketones. Herein, we first report a nickel-catalyzed cine-arylation of tert-cyclobutanols with indoles to access β-aryl ketones with an unusual site-selectivity at the C3-position of tert-cyclobutanols. The reaction features earth-abundant nickel catalysis, excellent regioselectivity, high atom-economy, and broad substrate scope.

Graphical abstract: Selective cine-arylation of tert-cyclobutanols with indoles enabled by nickel catalysis

Supplementary files

Article information

Article type
Communication
Submitted
07 Mar 2021
Accepted
05 Apr 2021
First published
06 Apr 2021

Chem. Commun., 2021,57, 4686-4689

Selective cine-arylation of tert-cyclobutanols with indoles enabled by nickel catalysis

Y. Hu, H. Luo, X. Tu, H. Xue, H. Jin, Y. Liu and B. Zhou, Chem. Commun., 2021, 57, 4686 DOI: 10.1039/D1CC01233A

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