Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 27th March 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.

Issue 10, 1997
Previous Article Next Article

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


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