Glaser oxidative coupling in ionic liquids: an improved synthesis of conjugated 1,3-diynes

Yadav, J. S. ; Reddy, B. V. S. ; Bhaskar Reddy, K. ; Uma Gayathri, K. ; Prasad, A. R. (2003) Glaser oxidative coupling in ionic liquids: an improved synthesis of conjugated 1,3-diynes Tetrahedron Letters, 44 (34). pp. 6493-6496. ISSN 0040-4039

Full text not available from this repository.

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

Related URL: http://dx.doi.org/10.1016/S0040-4039(03)01565-X

Abstract

Terminal alkynes undergo oxidative-coupling smoothly in the presence of the CuCl-TMEDA catalytic system in hydrophobic [bmim]PF6 ionic liquid under aerobic conditions to produce 1,3-diynes in excellent yields under mild conditions. The substrates, alkynes, show enhanced reactivity and selectivity in ionic liquids (ILs). The recovery of the catalyst is facilitated by the hydrophobic nature of the [bmim]PF6 ionic liquid.

Item Type:Article
Source:Copyright of this article belongs to Elsevier Science.
Keywords:Ionic Liquids (ILs); Alkynes; Oxidative-coupling; 1,3-diynes
ID Code:60400
Deposited On:09 Sep 2011 03:52
Last Modified:09 Sep 2011 03:52

Repository Staff Only: item control page