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

David P.G. Hamon; Kellie L. Tuck

doi:10.1039/a701756a

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

David P.G. Hamon, Kellie L. Tuck

Research output: Contribution to journal › Article › Research › peer-review

3 Citations (Scopus)

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.

Original language	English
Pages (from-to)	941-942
Number of pages	2
Journal	Chemical Communications
Issue number	10
DOIs	https://doi.org/10.1039/a701756a
Publication status	Published - 21 May 1997
Externally published	Yes

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title = "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.",

author = "Hamon, {David P.G.} and Tuck, {Kellie L.}",

year = "1997",

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AU - Tuck, Kellie L.

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JO - Chemical Communications

JF - Chemical Communications

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

Abstract

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