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  • Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol.

Selected regiocontrolled transformations applied to the synthesis of (1S)-cis-chrysanthemic acid from (1S)-3,4-epoxy-2,2,5,5-tetramethylcyclohexanol.

Chemical communications (Cambridge, England) (2008-10-03)
Alain Krief, Humaira Y Gondal, Adrian Kremer
ABSTRACT

(1S)-cis-Chrysanthemic acid has been prepared in a few steps with complete control of the relative and absolute stereochemistry using regiocontrolled epoxide ring opening, diol mono-oxidation and cyclopropanation.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
(+)-trans-Chrysanthemic acid, ≥97.0% (GC)