Issue 0, 1971

Lythraceous alkaloids. Part III. Synthesis of the product of dehydrogenation of dideoxy-NO-dimethyl-lythranidine; the structure of lythranidine

Abstract

A seventeen-membered heterocycle (VI), made from anisaldehyde by an eight-step synthesis, was shown to be identical with the product of dehydrogenation of dideoxy-NO-dimethyl-lythranidine. Lythranidine, a novel alkaloid from Lythrum anceps Makino, was thus assigned the structure (XV).

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 205-207

Lythraceous alkaloids. Part III. Synthesis of the product of dehydrogenation of dideoxy-NO-dimethyl-lythranidine; the structure of lythranidine

E. Fujita, K. Fuji and K. Tanaka, J. Chem. Soc. C, 1971, 205 DOI: 10.1039/J39710000205

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