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Issue 10, 1997
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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.

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

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    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

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