Synthesis of a functionalized allylic phosphine oxide

Article abstract of DOI:10.1080/00397919708005007

A functionalized allylic phosphine oxide has been prepared by regioselective bromination of 2-(methyldiphenylphosphinoyl)-1-propene followed by nucleophilic substitution with acetate. Hydrolysis and protection yielded the target compound.

Full text of DOI:10.1080/00397919708005007

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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Synthesis of a Functionalized
Allylic Phosphine Oxide
Michael Harmata a & Kevin W. Carter a
a Department of Chemistry, University of Missouri-
Columbia Columbia, Missouri, 65211
Published online: 22 Aug 2006.
To cite this article: Michael Harmata & Kevin W. Carter (1997): Synthesis of a
Functionalized Allylic Phosphine Oxide, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 27:17, 3027-3033
To link to this article: http://dx.doi.org/10.1080/00397919708005007
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