The stereochemistry of the product homoallylic alcohols from a modified grignard reaction of 3-phenylpropen-1-yl chloride and benzaldehyde
摘要：
The reaction of 3-phenylpropen-1-yl 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).
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DOI：
10.1016/S0040-4039(00)81673-1
被引量：
年份：
1983
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