Issue 14, 1978

Stereochemical control in the biomimetic conversion of heteroyohimbine alkaloid precursors. Isolation of a novel key intermediate

Abstract

The isolation of a novel key intermediate (3) related to cathenamine (4) and its conversion in a stereo-selective sequence of reactions into tetrahydroalstonine (8) and 19-epiajmalicine (10) afford new information concerning the biosynthesis of heteroyohimbine alkaloids.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1978, 618-619

Stereochemical control in the biomimetic conversion of heteroyohimbine alkaloid precursors. Isolation of a novel key intermediate

C. Kan-Fan and H. Husson, J. Chem. Soc., Chem. Commun., 1978, 618 DOI: 10.1039/C39780000618

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