Issue 15, 1985

Stereoselective synthesis of (+)-strictanonic acid, the enantiomer of a new type of diterpenoid, isolated from Grindelia stricta and Chrysothamnus paniculatus

Abstract

The synthesis of (+)-strictanonic acid (1a) from grindelic acid (2a)via the key intermediate (3a) is described; the synthesis confirms the proposed structure of (1a) and establishes its absolute stereochemistry.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1985, 1045-1046

Stereoselective synthesis of (+)-strictanonic acid, the enantiomer of a new type of diterpenoid, isolated from Grindelia stricta and Chrysothamnus paniculatus

M. G. Sierra, A. C. Olivieri, M. I. Colombo and E. A. Ruveda, J. Chem. Soc., Chem. Commun., 1985, 1045 DOI: 10.1039/C39850001045

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