Epoxydisilanes by direct double silylation of terminal epoxides
Terminal epoxides 2 are converted to epoxydisilanes 1 in a one-pot procedure in hexane at low temperatures, by using successive additions of Me3SiCl and s-BuLi-(-)-sparteine complex.
Hlavní autoři: | Hodgson, D, Kirton, E |
---|---|
Médium: | Journal article |
Jazyk: | English |
Vydáno: |
2004
|
Podobné jednotky
-
A remarkable base-induced rearrangement of epoxydisilanes
Autor: Hodgson, D, a další
Vydáno: (1996) -
Deprotonation-electrophile trapping of terminal epoxides.
Autor: Hodgson, D, a další
Vydáno: (2005) -
syn-β-Hydroxyallylic silanes from terminal epoxide α-lithiation-silylation and alkenylation: application to the tetrahydrofuran portion of the lytophilippines.
Autor: Hodgson, D, a další
Vydáno: (2012) -
Straightforward synthesis of alpha,beta-epoxysilanes from terminal epoxides by lithium 2,2,6,6-tetramethylpiperidide-mediated deprotonation-in situ silylation
Autor: Hodgson, D, a další
Vydáno: (2002) -
Substituted epoxides by lithiation of terminal epoxides.
Autor: Hodgson, D, a další
Vydáno: (2004)