Synthesis and biological evaluation of a des-dihydropyran laulimalide analog

Abstract

The preparation of a novel simplified Laulimalide analog via a highly convergent and efficient route and its biological evaluation are presented. The outlined route enables the synthesis of C 5–C 9 modified analog 2 and uses Julia–Kocienski olefination for fragment assembly and a regioselective Yamaguchi macrolactonization for ring closure. This strategy should be suitable for the generation of various new C 5–C 9 des-dihydropyran laulimalide derivatives for further SAR studies.