New Stereoselective Routes from Alcohols to Secondary Alkyl Bromides with Retention of Configuration

DOI: 10.1039/c39800000656

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 656 - 657 (1980)

Update date:2022-08-02

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Authors:

Sevrin, Mireille

Krief, Alain

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Article abstract of DOI:10.1039/c39800000656

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.

Full text of DOI:10.1039/c39800000656

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