| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5277332 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
Olefin self-cross-metathesis (CM) reactions catalyzed by the second-generation Grubbs carbene complex have been compared in dichloromethane and two kinds of selected room temperature ionic liquids (RTILs). Both the catalyst and the ionic liquids could be simply recovered and reused for at least four cycles just with a little drop in activity. Significant enhancements in the reactivity, yield and reaction rate were achieved.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Xiong Ding, Xianhai Lv, Bin Hui, Zhijuan Chen, Minliang Xiao, Baoshou Guo, Wenming Tang,