Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Org Chem ; 75(10): 3401-11, 2010 May 21.
Artigo em Inglês | MEDLINE | ID: mdl-20405933

RESUMO

Diethylaminodifluorosulfinium tetrafluoroborate (XtalFluor-E) and morpholinodifluorosulfinium tetrafluoroborate (XtalFluor-M) are crystalline fluorinating agents that are more easily handled and significantly more stable than Deoxo-Fluor, DAST, and their analogues. These reagents can be prepared in a safer and more cost-efficient manner by avoiding the laborious and hazardous distillation of dialkylaminosulfur trifluorides. Unlike DAST, Deoxo-Fluor, and Fluolead, XtalFluor reagents do not generate highly corrosive free-HF and therefore can be used in standard borosilicate vessels. When used in conjunction with promoters such as Et(3)N.3HF, Et(3)N.2HF, or DBU, XtalFluor reagents effectively convert alcohols to alkyl fluorides and carbonyls to gem-difluorides. These reagents are typically more selective than DAST and Deoxo-Fluor and exhibit superior performance by providing significantly less elimination side products.


Assuntos
Boratos/química , Hidrocarbonetos Fluorados/química , Morfolinas/química , Compostos de Enxofre/química , Temperatura , Boratos/síntese química , Halogenação , Hidrocarbonetos Fluorados/síntese química , Estrutura Molecular , Morfolinas/síntese química , Sais/síntese química , Sais/química , Estereoisomerismo , Compostos de Enxofre/síntese química
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...