Indium(I) iodide promoted highly selective 1,2-addition of allyl and benzyl groups to α,β-unsaturated nitriles under sonication: a new synthesis of conjugated imines

Ranu, Brindaban C. ; Das, Arijit (2004) Indium(I) iodide promoted highly selective 1,2-addition of allyl and benzyl groups to α,β-unsaturated nitriles under sonication: a new synthesis of conjugated imines Tetrahedron Letters, 45 (37). pp. 6875-6877. ISSN 0040-4039

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Official URL: http://linkinghub.elsevier.com/retrieve/pii/S00404...

Related URL: http://dx.doi.org/10.1016/j.tetlet.2004.07.098

Abstract

Allyl and benzyl bromides react with α, β- unsaturated nitriles in the presence of indium(I) iodide under sonication to produce the corresponding allylated and benzylated conjugated imines involving exclusive addition of the allyl/benzyl group to the C≡N moiety.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Indium(I) Iodide; Conjugated Nitrile; 1,2-addition; Imine; Sonication
ID Code:41702
Deposited On:31 May 2011 04:52
Last Modified:31 May 2011 04:52

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