Issue 3, 1994

Efficient synthesis of 6-prenylcoumarins; total syntheses of suberosin, toddaculin, O-methylapigravin (O-methylbrosiperin) and O-methylbalsamiferone

Abstract

Synthesis of naturally occuring 6-prenylcoumarins 1a, b, 2c, and 3b and their derivatives 6ac is described, starting from 2-prenyloxybenzaldehydes 4ac, using a tandem Claisen rearrangement and Wittig reaction.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1994, 251-252

Efficient synthesis of 6-prenylcoumarins; total syntheses of suberosin, toddaculin, O-methylapigravin (O-methylbrosiperin) and O-methylbalsamiferone

R. S. Mali, P. K. Sandhu and A. Manekar-Tilve, J. Chem. Soc., Chem. Commun., 1994, 251 DOI: 10.1039/C39940000251

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