4.4 Article

Total synthesis of the antitumor agent (-)-laulimalide

Journal

TETRAHEDRON LETTERS
Volume 43, Issue 18, Pages 3381-3383

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0040-4039(02)00472-0

Keywords

marine metabolites; antitumor compounds; macrolactonization; allylsilane addition; chiral acetal

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A stereocontrolled synthesis of the title compound is described. Key steps are an allylsilane addition to a chiral acetal as the major coupling step and a Yamaguchi macrolactonization for ring closure. (C) 2002 Elsevier Science Ltd. All rights reserved.

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