Issue 12, 2019

Metal-free, radical 1,6-conjugated addition of cyclic ethers with para-quinone methides (p-QMs)

Abstract

An efficient method for metal-free C–C bond formation between p-quinone methides (p-QMs) and cyclic ethers via a radical pathway to afford substituted diarylmethanes and triarylmethanes or to effect the α-alkylation of the cyclic ethers has been developed. Also, the synthesis of 3,3′-disubstituted oxindoles with stereogenic quaternary carbon centers was successfully achieved under mild reaction conditions.

Graphical abstract: Metal-free, radical 1,6-conjugated addition of cyclic ethers with para-quinone methides (p-QMs)

Supplementary files

Article information

Article type
Paper
Submitted
17 Jan 2019
Accepted
19 Feb 2019
First published
19 Feb 2019

Org. Biomol. Chem., 2019,17, 3239-3248

Metal-free, radical 1,6-conjugated addition of cyclic ethers with para-quinone methides (p-QMs)

S. G. More and G. Suryavanshi, Org. Biomol. Chem., 2019, 17, 3239 DOI: 10.1039/C9OB00127A

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