| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1315125 | Journal of Fluorine Chemistry | 2010 | 4 Pages |
Abstract
A convenient lithium bromide/triethylamine promoted tandem cycloaddition–oxidation reaction was developed to afford 3-trifluoroacetyl pyrroles in moderate to good yields from N-alkylidene 2-amino esters and β-trifluoroacetyl vinyl ethyl ether.
Graphical abstractA convenient lithium bromide/triethylamine promoted tandem cycloaddition–oxidation reaction was developed to afford 3-trifluoroacetyl pyrroles in moderate to good yields from N-alkylidene 2-amino esters and β-trifluoroacetyl vinyl ethyl ether.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Yong Xin, Jingwei Zhao, Jianwei Han, Shizheng Zhu,