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Communication | Special issue | Vol 42, No. 2, 1996, pp.509-512
Published online, 1st January, 1970
DOI: 10.3987/COM-95-S81
Syntheses of Proposed Structure of Pseudodistomin A Triacetate and Its Regioisomers on Dienyl Side-Chain

Toshiko Kiguchi, Yoko Yuumoto, Ichiya Ninomiya, and Takeaki Naito

*Kobe Pharmaceutical University, Motoyamakita, Higashinada, Kobe 658-8558, Japan

Abstract

The amino alcohol (5) was employed as a common starting compound for the synthesis of the piperidines (1b), (14), and (16) with three isomeric tridecadienyl side-chains. The spectral data of the 6’E,8’Z-diene (14) are closely resembled with those of natural pseudodistomin A triacetate.