Total Synthesis of (−) and (+)-Zingibergingerols A

Abstract

The first total synthesis of both of the enantiomers of Zingibergingerol A has been accomplished. The distinctive 3,7,9trioxabicyclo[4.2.1]nonane skeleton is crafted through goldcatalyzed alkynol cycloisomerization. The synthesis comprises sequential C−C bond formations at both ends of epichlorohydrin: first opening the epoxide with eugenol-derived alkyne, followed by subsequent epoxide installation, and again opening with a Grignard reagent. The resulting alkynol with a fixed C5 stereochemistry was subjected to O-allylation, followed by dihydroxylation and alkynol cycloisomerization.Note pubs.acs.org/joc