Issue 12, 1994

Efficient optical resolution of cis-4-methylcyclohex-4-ene-1,2-dicarboxylic anhydride, cis-4- methylcyclohex-4-ene-1,2-dicarboximide, and their derivatives by complexation with optically active host compounds derived from tartaric acid

Abstract

Optically pure enantiomers of cis-4-methylcyclohex-4-ene-1,2-dicarboxylic anhydrides, cis-4-methylcyclohex-4-ene-1,2-dicarboximides and 3-oxabicyclo[4.3.0]non-7-en-2-ones have been obtained by optical resolution through enantioselective inclusion complexation with optically active host compounds derived from tartaric acid. Kinetic resolution of cyclohex-4-ene-1,2-dicarboximides and cyclohexane-1,2-dicarboximides by way of enantioselective hydrolysis is also reported.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1994, 1601-1604

Efficient optical resolution of cis-4-methylcyclohex-4-ene-1,2-dicarboxylic anhydride, cis-4- methylcyclohex-4-ene-1,2-dicarboximide, and their derivatives by complexation with optically active host compounds derived from tartaric acid

F. Toda, H. Miyamoto and H. Ohta, J. Chem. Soc., Perkin Trans. 1, 1994, 1601 DOI: 10.1039/P19940001601

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