Catalysis by ionic liquids: cyclopropyl carbinyl rearrangements catalyzed by [pmim]Br under organic solvent free conditions

Ranu, Brindaban C. ; Banerjee, Subhash ; Das, Arijit (2006) Catalysis by ionic liquids: cyclopropyl carbinyl rearrangements catalyzed by [pmim]Br under organic solvent free conditions Tetrahedron Letters, 47 (6). pp. 881-884. 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.2005.12.003

Abstract

Aryl substituted cyclopropyl carbinol derivatives undergo stereoselective rearrangements catalyzed by the ionic liquid, 1-methyl-3-pentylimidazolium bromide, under sonication, without any organic solvent, to produce the substituted conjugated all-trans-butadienes.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Ionic Liquid; Catalysis; Rearrangement; Cyclopropyl Carbinol; Butadienes
ID Code:41481
Deposited On:30 May 2011 05:17
Last Modified:30 May 2011 05:17

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