| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 171033 | Comptes Rendus Chimie | 2011 | 5 Pages |
Abstract
A novel, clean and efficient tandem process has been established for the synthesis of 2,4,6-triarylpyridines from primary aryl alcohols or 1-arylethanols using 1-methylimidazolium nitrate in 1-butyl-3-methylimidazolium tetrafluoroborate as a binary task-specific ionic liquid under microwave irradiation.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
Ahmad R. Khosropour, Iraj Mohammadpoor-Baltork, Forough Kiani,
![First Page Preview: Green, new and efficient tandem oxidation and conversion of aryl alcohols to 2,4,6-triarylpyridines promoted by [HMIm]NO3-[BMIm]BF4 as a binary ionic liquid Green, new and efficient tandem oxidation and conversion of aryl alcohols to 2,4,6-triarylpyridines promoted by [HMIm]NO3-[BMIm]BF4 as a binary ionic liquid](/preview/png/171033.png)