Issue 29, 2022

Visible light-induced selenylative spirocyclization of biaryl ynones toward the formation of selenated spiro[5.5]trienones

Abstract

A visible-light induced dearomative cascade cyclization of biaryl ynones with diselenides under photocatalyst and external additive-free conditions has been explored, giving a series of selenated spiro[5.5]trienones in moderate to good yields. The Se–Se bond in diselenides could be cleaved to generate arylselenyl radicals under visible light irradiation in the absence of a photocatalyst. This protocol provides a facile and green method for the synthesis of spiro[5.5]trienones.

Graphical abstract: Visible light-induced selenylative spirocyclization of biaryl ynones toward the formation of selenated spiro[5.5]trienones

Supplementary files

Article information

Article type
Paper
Submitted
26 May 2022
Accepted
27 Jun 2022
First published
28 Jun 2022

Org. Biomol. Chem., 2022,20, 5779-5783

Visible light-induced selenylative spirocyclization of biaryl ynones toward the formation of selenated spiro[5.5]trienones

Z. Chen, X. Zheng, S. Zhou and X. Cui, Org. Biomol. Chem., 2022, 20, 5779 DOI: 10.1039/D2OB01006B

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