All-carbon-substituted vinylsilane stable to TBAF: synthesis of allyldimethylvinylsilane and its Pd-catalyzed cross-coupling under mild conditions.
Org Lett
; 8(17): 3733-6, 2006 Aug 17.
Article
en En
| MEDLINE
| ID: mdl-16898804
[reaction: see text] Allyldimethylvinylsilanes 3 are easily synthesized by the reaction of silylallylmetals, generated from 1 by n-BuLi/t-BuOK, with carbonyl compounds in the absence or presence of metal halides. They can tolerate 2 equiv of TBAF in THF at room temperature for at least 6 h but can be easily activated in the presence of a palladium catalyst and TBAF to perform the cross-coupling reaction with aryl iodides at room temperature.
Buscar en Google
Bases de datos:
MEDLINE
Idioma:
En
Revista:
Org Lett
Asunto de la revista:
BIOQUIMICA
Año:
2006
Tipo del documento:
Article