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Issue 10, 1997
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A concise asymmetric synthesis of the pheromone 1-methylcyclohex-2-enol via a ‘merged substitution-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.

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Article information


Chem. Commun., 1997, 941-942
Article type
Paper

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, 941
DOI: 10.1039/A701756A

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