Issue 58, 2024

Asymmetric dearomatization of benzyl 1-naphthyl ethers via [1,3] O-to-C rearrangement

Abstract

A catalytic asymmetric dearomatization reaction of benzyl 1-naphthyl ethers accelerated by a chiral N,N′-dioxide/Co(II) complex is disclosed. The reaction proceeds via an enantioselective [1,3] O-to-C rearrangement through a tight ion-pair pathway, providing a wide array of α-naphthalenone derivatives bearing an all-carbon quaternary center in high yields with excellent ee values.

Graphical abstract: Asymmetric dearomatization of benzyl 1-naphthyl ethers via [1,3] O-to-C rearrangement

Supplementary files

Article information

Article type
Communication
Submitted
30 May 2024
Accepted
19 Jun 2024
First published
20 Jun 2024

Chem. Commun., 2024,60, 7507-7510

Asymmetric dearomatization of benzyl 1-naphthyl ethers via [1,3] O-to-C rearrangement

H. Zeng, G. Wen, L. Lin and X. Feng, Chem. Commun., 2024, 60, 7507 DOI: 10.1039/D4CC02620A

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