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...

पूर्ण विवरण

ग्रंथसूची विवरण
मुख्य लेखकों:	Hodgson, D, Stefane, B, Miles, T, Witherington, J
स्वरूप:	Journal article
भाषा:	English
प्रकाशित:	2006

समान संसाधन

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Unsaturated 1,2-amino alcohols from dihydropyrrole epoxides and organolithiums
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Metalated Epoxides and Aziridines in Synthesis
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Widening the usefulness of epoxides and aziridines in synthesis
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Studies on organolithium-induced alkylative desymmetrisation of epoxides: synthesis of enantioenriched beta-amino cycloheptenols from 6,7-epoxy-8-azabicyclo[3.2.1]octanes (vol, 60 pg, 5185 2004)
द्वारा: Hodgson, D, और अन्य
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Erratum: Studies on organolithium-induced alkylative desymmetrisation of epoxides: Synthesis of enantioenriched β-amino cycloheptenols from 6,7-epoxy-8-azabicyclo[3.2.1]octanes (Tetrahedron (2004) 60 (5185))
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Widening the usefulness of epoxides and aziridines in synthesis
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