Issue 7, 1995

Synthesis and stereochemistry of optically active telluronium ylides

Abstract

Diastereoisomeric mixtures of 1-{4-[(–)-menthyloxycarbonyl]phenyl(methyl)telluroniumyl}-4,4-dimethyl-2,6-dioxocyclohexan-1-ide dia.-5a, b and 1-{4[(–)-menthyloxycarbonyl]phenyl(2,4,6-triisopropylphenyl)-telluroniumyl}-4,4-dimethyl-2,6-dioxocyclohexan-1-ide dia.-12a, b have been synthesized. Optical resolution by the fractional recrystallization of dia.-5a, b and dia.-12a, b from hexane–dichloromethane gave the optically active (+)Te-telluronium ylides (+)Te-5a and (+)Te-12a as stable crystals, respectively. The absolute configuration of (+)Te-5a has been determined to be R based on the CD spectrum. The kinetics for the epimerization by pyramidal inversion of the optically active telluronium ylide (+)Te-12a have been studied.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1995, 821-827

Synthesis and stereochemistry of optically active telluronium ylides

N. Kamigata, A. Matsuhisa, H. Taka and T. Shimizu, J. Chem. Soc., Perkin Trans. 1, 1995, 821 DOI: 10.1039/P19950000821

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