Issue 10, 1990

Homochiral syntheses of (–)-dihydrocorynantheol

Abstract

A Corynanthe-type indole alkaloid, (–)-dihydrocorynantheol (7), was enantioselectively synthesized from (+)-(4S,5R)-4-(2-benzyloxyethyl)-5-ethyl-3,4,5,6-tetrahydro-2-pyrone (3), derived from ethylmalonic acid. The synthetic compound (7) was identical in all respects with a sample prepared from yohimbine (8).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 2771-2773

Homochiral syntheses of (–)-dihydrocorynantheol

M. Ihara, N. Taniguchi, K. Yasui and K. Fukumoto, J. Chem. Soc., Perkin Trans. 1, 1990, 2771 DOI: 10.1039/P19900002771

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