Organolithium-induced alkylative ring opening of aziridines: synthesis of unsaturated amino alcohols and ethers.

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...

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Bibliografiske detaljer
Main Authors:	Hodgson, D, Stefane, B, Miles, T, Witherington, J
Format:	Journal article
Sprog:	English
Udgivet:	2006

Lignende værker

Unsaturated 1,2-amino alcohols and ethers from aziridines and organolithiums.
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Organolithium methods /
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