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

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Résumé

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.

langue originale	Anglais
Pages (de - à)	656-657
Nombre de pages	2
journal	Journal of the Chemical society. Chemical communications
Numéro de publication	14
Les DOIs	https://doi.org/10.1039/C39800000656
Etat de la publication	Publié - 1 janv. 1980

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10.1039/C39800000656

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title = "New stereoselective routes from alcohols to secondary alkyl bromides with retention of configuration",

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.",

author = "M. Sevrin and A. Krief",

year = "1980",

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doi = "10.1039/C39800000656",

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pages = "656--657",

journal = "Journal of the Chemical society. Chemical communications",

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AU - Krief, A.

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

Résumé

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