Catalytic oxidative cyclization of α-carbonyl-γ-alkynyl sulfoxonium ylides for stereospecific synthesis of (1Z,3Z)-1,3-bismethyleneisobenzofurans

Abstract

A new copper(II)-catalyzed annulation-enabled radical addition cascade of α-carbonyl-γ-alkynyl sulfoxonium ylides with sulfonyl hydrazides in the presence of tert-butyl hydroperoxide (TBHP) is reported, enabling a completely regio- and stereoselective strategy to access (1Z,3Z)-1,3-bismethyleneisobenzofurans in moderate-to-good yields. The protocol features a good substrate scope and functional group tolerance and proceeds through regioselective 5-exo-dig oxo-cyclization followed by stereoselective radical addition reaction.

Graphical abstract: Catalytic oxidative cyclization of α-carbonyl-γ-alkynyl sulfoxonium ylides for stereospecific synthesis of (1Z,3Z)-1,3-bismethyleneisobenzofurans

Supplementary files

Article information

Article type
Research Article
Submitted
23 Apr 2024
Accepted
10 May 2024
First published
10 May 2024

Org. Chem. Front., 2024, Advance Article

Catalytic oxidative cyclization of α-carbonyl-γ-alkynyl sulfoxonium ylides for stereospecific synthesis of (1Z,3Z)-1,3-bismethyleneisobenzofurans

P. Zhou, W. Yang, W. Hao and B. Jiang, Org. Chem. Front., 2024, Advance Article , DOI: 10.1039/D4QO00735B

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