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The stereochemistry of the product homoallylic alcohols from a modified grignard reaction of 3-phenylpropen-1-yl chloride and benzaldehyde.

✍ Scribed by James M. Coxon; Gregory W. Simpson; Peter J. Steel; V.Craige Trenerry


Book ID
104217123
Publisher
Elsevier Science
Year
1983
Tongue
French
Weight
123 KB
Volume
24
Category
Article
ISSN
0040-4039

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✦ Synopsis


The reaction of 3-phenylpropen-l-y1 magnesium chloride with benzaldehyde gave a mixture (7:3) of homoallylic alcohols (1) and (2) the relative configuration of which was determined from an X-ray analysis of the major epoxide formed by m-chloroperbenzoic oxidation of alcohol (1).