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A selective C–H insertion/olefination protocol for the synthesis of α-methylene-γ-butyrolactone natural products†
Matthew G. Lloyd,Mariantonietta D'Acunto,Richard J. K. Taylor,William P. Unsworth
Organic & Biomolecular Chemistry Pub Date : 12/17/2015 00:00:00 , DOI:10.1039/C5OB02579F
Abstract

A regio- and stereoselective one-pot C–H insertion/olefination protocol has been developed for the late stage installation of α-methylene-γ-butyrolactones into conformationally restricted cyclohexanol-derivatives. The method has been successfully applied in the total synthesis of eudesmanolide natural product frameworks, including α-cyclocostunolide.

Graphical abstract: A selective C–H insertion/olefination protocol for the synthesis of α-methylene-γ-butyrolactone natural products
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