Structure and conformation of α′-diphenylphosphinoyl enones: X-ray structure of E-(5SR,6SR)-3,6-dimethyl-5-diphenylphosphinoyl-7- triphenylmethoxyhept-2-en-4-one

Michael J. Doyle; David Hall; Paul R. Raithby; Nicholas Skelton; Stuart Warren

doi:10.1039/p19930000517

Structure and conformation of α′-diphenylphosphinoyl enones: X-ray structure of E-(5SR,6SR)-3,6-dimethyl-5-diphenylphosphinoyl-7- triphenylmethoxyhept-2-en-4-one

Michael J. Doyle
, David Hall
, Paul R. Raithby
, Nicholas Skelton
, Stuart Warren

University of Cambridge

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

Abstract

A series of α′-diphenylphosphinoyl enones has been prepared and their s-cis or s-trans conformations correlated with ¹H NMR and IR spectra and an X-ray crystal structure of the title compound. The effect of chelation to cerium(III) is correlated with the regio- and stereo-selectivity of reductions under the Luche conditions.

Original language	English
Pages (from-to)	517-523
Number of pages	7
Journal	Journal of the Chemical Society, Perkin Transactions 1
Issue number	4
DOIs	https://doi.org/10.1039/p19930000517
Publication status	Published - 1993

ASJC Scopus subject areas

General Chemistry

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10.1039/p19930000517

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Structure and conformation of α′-diphenylphosphinoyl enones: X-ray structure of E-(5SR,6SR)-3,6-dimethyl-5-diphenylphosphinoyl-7- triphenylmethoxyhept-2-en-4-one. / Doyle, Michael J.; Hall, David; Raithby, Paul R. et al.
In: Journal of the Chemical Society, Perkin Transactions 1, No. 4, 1993, p. 517-523.

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

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abstract = "A series of α′-diphenylphosphinoyl enones has been prepared and their s-cis or s-trans conformations correlated with 1H NMR and IR spectra and an X-ray crystal structure of the title compound. The effect of chelation to cerium(III) is correlated with the regio- and stereo-selectivity of reductions under the Luche conditions.",

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AU - Skelton, Nicholas

AU - Warren, Stuart

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AB - A series of α′-diphenylphosphinoyl enones has been prepared and their s-cis or s-trans conformations correlated with 1H NMR and IR spectra and an X-ray crystal structure of the title compound. The effect of chelation to cerium(III) is correlated with the regio- and stereo-selectivity of reductions under the Luche conditions.

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Structure and conformation of α′-diphenylphosphinoyl enones: X-ray structure of E-(5SR,6SR)-3,6-dimethyl-5-diphenylphosphinoyl-7- triphenylmethoxyhept-2-en-4-one

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