Scandium triflate-catalyzed 1,3-dipolar cycloaddition of aziridines with alkenes

Yadav, J. S. ; Subba Reddy, B. V. ; Pandey, Sushil Kumar ; Srihari, P. ; Prathap, I. (2001) Scandium triflate-catalyzed 1,3-dipolar cycloaddition of aziridines with alkenes Tetrahedron Letters, 42 (51). pp. 9089-9092. ISSN 0040-4039

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Official URL: http://www.sciencedirect.com/science/article/pii/S...

Related URL: http://dx.doi.org/10.1016/S0040-4039(01)02008-1

Abstract

Phenyl aziridines undergo 1,3-dipolar cycloaddition efficiently with olefins such as cyclic enol ethers and allyltrimethylsilane in the presence of a catalytic amount of Sc(OTf)3 at ambient temperature to afford the corresponding pyrrolidine derivatives in high yields with high regioselectivity.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Aziridines; Scandium Triflate; Cycloaddition; Pyrrolidines
ID Code:58856
Deposited On:02 Sep 2011 03:11
Last Modified:02 Sep 2011 03:11

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