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...
Những tác giả chính: | Hodgson, D, Stefane, B, Miles, T, Witherington, J |
---|---|
Định dạng: | Journal article |
Ngôn ngữ: | English |
Được phát hành: |
2006
|
Những quyển sách tương tự
-
Unsaturated 1,2-amino alcohols and ethers from aziridines and organolithiums.
Bằng: Hodgson, D, et al.
Được phát hành: (2004) -
Organolithium-induced enantioselective alkylative double ring-opening of epoxides: synthesis of enantioenriched unsaturated amino alcohols
Bằng: Hodgson, D, et al.
Được phát hành: (2004) -
Organolithium-induced synthesis of acyclic unsaturated amino alcohols from epoxides of dihydropyrroles and tetrahydropyridines
Bằng: Hodgson, D, et al.
Được phát hành: (2003) -
Unsaturated 1,2-amino alcohols from dihydropyrrole epoxides and organolithiums
Bằng: Hodgson, D, et al.
Được phát hành: (2002) -
Enantioselective alkylative double ring opening of epoxides: synthesis of enantioenriched unsaturated diols and amino alcohols.
Bằng: Hodgson, D, et al.
Được phát hành: (2002)