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Synthesis of a bicyclic model for the marine hepatotoxin cylindrospermopsin
Journal article   Peer reviewed

Synthesis of a bicyclic model for the marine hepatotoxin cylindrospermopsin

Barry B Snider and Thomas C Harvey
Tetrahedron letters, Vol.36(26), pp.4587-4590
06/26/1995

Abstract

A double Michael addition of ammonia to dienone 9 to give piperidinone 10 and the reaction of diamine 16 with isothiocyanate 19 to give protected guanidine 18 are the key transformations in a ten-step synthesis of the cylindrospermopsin model 22.

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