Asymmetric Synthesis of Scillascillin-Type Homoisoflavonoid

Org Lett. 2024 Feb 2;26(4):834-838. doi: 10.1021/acs.orglett.3c03968. Epub 2024 Jan 19.

Abstract

The first asymmetric synthesis of a scillascillin-type homoisoflavonoid was reported. Key reactions for the asymmetric synthesis of benzocyclobutene include catalytic reductive desymmetrization of malonic ester and an intramolecular C-H activation of the methyl group.