Jump to main content
Jump to site search

Issue 10, 1997
Previous Article Next Article

A concise asymmetric synthesis of the pheromone1-methylcyclohex-2-enol via a ‘mergedsubstitution-elimination reaction’

Abstract

The title compound is prepared (>94% ee) by a three step synthesis from 1-methylcyclohexene via a ‘merged substitution-elimination reaction’ involving a phenylselenide ion.

Back to tab navigation

Article type: Paper
DOI: 10.1039/A701756A
Citation: Chem. Commun., 1997,0, 941-942
  •   Request permissions

    A concise asymmetric synthesis of the pheromone 1-methylcyclohex-2-enol via a ‘merged substitution-elimination reaction’

    D. P. G. Hamon and K. L. Tuck, Chem. Commun., 1997, 0, 941
    DOI: 10.1039/A701756A

Search articles by author

Spotlight

Advertisements