Organolithium-induced alkylative ring opening of aziridines: synthesis of unsaturated amino alcohols and ethers.
Organolithium-induced alkylative ring opening of N-sulfonyl-protected aziridinyl ethers is described. The reactions were efficiently carried out with a variety of organolithiums, providing a promising new strategy to unsaturated amino alcohols and ethers. Cis- and trans-1,4-dimethoxybut-2-ene-derive...
المؤلفون الرئيسيون: | Hodgson, D, Stefane, B, Miles, T, Witherington, J |
---|---|
التنسيق: | Journal article |
اللغة: | English |
منشور في: |
2006
|
مواد مشابهة
-
Unsaturated 1,2-amino alcohols and ethers from aziridines and organolithiums.
حسب: Hodgson, D, وآخرون
منشور في: (2004) -
Organolithium-induced enantioselective alkylative double ring-opening of epoxides: synthesis of enantioenriched unsaturated amino alcohols
حسب: Hodgson, D, وآخرون
منشور في: (2004) -
Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines
حسب: Hodgson, D, وآخرون
منشور في: (2003) -
Unsaturated 1,2-amino alcohols from dihydropyrrole epoxides and organolithiums
حسب: Hodgson, D, وآخرون
منشور في: (2002) -
Enantioselective alkylative double ring opening of epoxides: synthesis of enantioenriched unsaturated diols and amino alcohols.
حسب: Hodgson, D, وآخرون
منشور في: (2002)