Tetrahedron

Enantioselective total synthesis of δ-lactonic marine natural products,(+)-tanikolide and (−)-malyngolide, via RCM reaction

H Mizutani, M Watanabe, T Honda

Index: Mizutani, Hirotake; Watanabe, Masayuki; Honda, Toshio Tetrahedron, 2002 , vol. 58, # 44 p. 8929 - 8936

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Citation Number: 60

Abstract

Download PDF Opens in a new window. Article suggestions will be shown in a dialog on return to ScienceDirect. ... Please enable JavaScript to use all the features on this page. ... Enantioselective total synthesis of δ-lactonic marine natural products, (+)-tanikolide and (−)-malyngolide isolated from Lyngbya majuscula, was achieved by using the Sharpless asymmetric epoxidation and a ring-closing metathesis, as key reactions. ... Structures (+)-tanikolide and ...