Journal of Organic Chemistry p. 5851 - 5856 (1992)
Update date:2022-08-04
Topics:
Marshall, James A.
Andersen, Marc W.
The diastereomerically labeled d1 enals 1 and 2 were prepared from (S)-3-bromo-2-methylpropanol 5 by a sequence involving homologation to the allylic alcohol 13 and Sharpless epoxidation to either the α- or the β-epoxide diastereomers 14 or 15.Reduction w
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