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Org Lett ; 14(10): 2626-9, 2012 May 18.
Artigo em Inglês | MEDLINE | ID: mdl-22571722

RESUMO

A convenient and efficient procedure is described for the sulfamoylation of alcohols using N-(tert-butoxycarbonyl)-N-[(triethylenediammonium)sulfonyl]azanide (1). The ambient temperature stable reagent 1 reacts with phenols as well as primary and secondary alcohols to give high to modest yields. The relative reaction rate of substrates was determined (primary > phenol > secondary ≫ tertiary). The reagent's utility as a selective sulfamoylation reagent with polyols is also demonstrated.


Assuntos
Álcoois/química , Sulfonas/química , Aminas , Indicadores e Reagentes , Estrutura Molecular , Fenóis
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