New stereoselective routes from alcohols to secondary alkyl bromides with retention of configuration
- 1 January 1980
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 14,p. 656-657
- https://doi.org/10.1039/c39800000656
Abstract
Secondary alcohols can be converted into the corresponding bromides with high stereoselective retention of configuration; this two-step process proceeds by a double inversion involving the intermediate selenides.Keywords
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