Applications of the stereochemically-controlled Horner-Wittig reaction: Synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene

Antony D. Buss; Nicholas Greeves; Ralph Mason; Stuart Warren

doi:10.1039/p19870002569

Applications of the stereochemically-controlled Horner-Wittig reaction: Synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene

Antony D. Buss, Nicholas Greeves, Ralph Mason, Stuart Warren

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

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Abstract

Stereoselective reduction of the appropriate α-diphenylphosphinoyl ketone or addition of the lithium derivative of an alkyl diphenylphosphine oxide to an aldehyde or a ketone gives Horner-Wittig intermediates and hence the title compounds.

Original language	English (US)
Pages (from-to)	2569-2577
Number of pages	9
Journal	Journal of the Chemical Society, Perkin Transactions 1
DOIs	https://doi.org/10.1039/p19870002569
State	Published - 1987

ASJC Scopus subject areas

General Chemistry

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Buss, A. D., Greeves, N., Mason, R., & Warren, S. (1987). Applications of the stereochemically-controlled Horner-Wittig reaction: Synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene. Journal of the Chemical Society, Perkin Transactions 1, 2569-2577. https://doi.org/10.1039/p19870002569

Applications of the stereochemically-controlled Horner-Wittig reaction: Synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene. / Buss, Antony D.; Greeves, Nicholas; Mason, Ralph et al.
In: Journal of the Chemical Society, Perkin Transactions 1, 1987, p. 2569-2577.

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

Buss, AD, Greeves, N, Mason, R & Warren, S 1987, 'Applications of the stereochemically-controlled Horner-Wittig reaction: Synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene', Journal of the Chemical Society, Perkin Transactions 1, pp. 2569-2577. https://doi.org/10.1039/p19870002569

Buss AD, Greeves N, Mason R, Warren S. Applications of the stereochemically-controlled Horner-Wittig reaction: Synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene. Journal of the Chemical Society, Perkin Transactions 1. 1987;2569-2577. doi: 10.1039/p19870002569

Buss, Antony D. ; Greeves, Nicholas ; Mason, Ralph et al. / Applications of the stereochemically-controlled Horner-Wittig reaction : Synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene. In: Journal of the Chemical Society, Perkin Transactions 1. 1987 ; pp. 2569-2577.

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abstract = "Stereoselective reduction of the appropriate α-diphenylphosphinoyl ketone or addition of the lithium derivative of an alkyl diphenylphosphine oxide to an aldehyde or a ketone gives Horner-Wittig intermediates and hence the title compounds.",

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Applications of the stereochemically-controlled Horner-Wittig reaction: Synthesis of feniculin, (E)-non-6-en-1-ol, a pheromone of the mediterranean fruit fly, (E)- and (Z)-dec-5-en-1-ol, tri-substituted alkenes, and (Z)-α-bisabolene

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