Issue 13, 2022

A formal [4 + 1] cycloaddition reaction of Baylis–Hillman bromides with sulfur ylides: facile access to α-alkenyl lactones

Abstract

A formal [4 + 1] cycloaddition reaction of Baylis–Hillman adducts with sulfur ylides has been developed for the first time. This protocol features high functional group tolerance and provides facile access to biologically interesting α-alkenyl lactones with generally high yields. Meanwhile, the DFT calculation of the pathways has also been performed.

Graphical abstract: A formal [4 + 1] cycloaddition reaction of Baylis–Hillman bromides with sulfur ylides: facile access to α-alkenyl lactones

Supplementary files

Article information

Article type
Research Article
Submitted
25 Mar 2022
Accepted
17 May 2022
First published
19 May 2022

Org. Chem. Front., 2022,9, 3558-3564

A formal [4 + 1] cycloaddition reaction of Baylis–Hillman bromides with sulfur ylides: facile access to α-alkenyl lactones

T. Hua, Y. Ma, X. He, L. Wang, J. Yan and Q. Yang, Org. Chem. Front., 2022, 9, 3558 DOI: 10.1039/D2QO00451H

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