New stereoselective routes from alcohols to secondary alkyl bromides with retention of configuration

M. Sevrin; A. Krief

doi:10.1039/C39800000656

New stereoselective routes from alcohols to secondary alkyl bromides with retention of configuration

Research output: Contribution to journal › Article › peer-review

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.

Original language	English
Pages (from-to)	656-657
Number of pages	2
Journal	Journal of the Chemical society. Chemical communications
Issue number	14
DOIs	https://doi.org/10.1039/C39800000656
Publication status	Published - 1 Jan 1980

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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.",

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New stereoselective routes from alcohols to secondary alkyl bromides with retention of configuration

Abstract

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