Issue 2, 1997

Synthesis of sphingosine relatives. Part 19.1 Synthesis of penaresidin A and B, azetidine alkaloids with actomyosin ATPase-activating properties

Abstract

Three stereoisomers of penaresidin A 1 and two stereoisomers of penaresidin B 2′ (Scheme 5), azetidine alkaloids isolated from the Okinawan marine sponge Penares sp., have been synthesized. In the course of our synthetic study, the correct structure of penaresidin B has been shown to be not 2 but 2′. Natural penaresidin A is either (2S,3R,4S,15S,16S)- or (2S,3R,4S,15R,16R)-1 and natural penaresidin B is either (2S,3R,4S,15S)- or (2S,3R,4S,15R)-2′.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 97-112

Synthesis of sphingosine relatives. Part 19.1 Synthesis of penaresidin A and B, azetidine alkaloids with actomyosin ATPase-activating properties

H. Takikawa, T. Maeda, M. Seki, H. Koshino and K. Mori, J. Chem. Soc., Perkin Trans. 1, 1997, 97 DOI: 10.1039/A604276G

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