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A stereoselective total synthesis of 7,8-O-isopropylidene iriomoteolide-3a†
Yao Zhang,Lisheng Deng,Gang Zhao
Organic & Biomolecular Chemistry Pub Date : 03/30/2011 00:00:00 , DOI:10.1039/C0OB01253J
Abstract

A stereoselective total synthesis of 7,8-O-isopropylidene iriomoteolide-3a has been achieved by using Yamaguchi esterification, Julia–Kocienski olefination, organocatalytic α-oxidation, and ring-closing metathesis reaction as key bond-forming steps.

Graphical abstract: A stereoselective total synthesis of 7,8-O-isopropylidene iriomoteolide-3a
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