| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1254637 | Chinese Chemical Letters | 2012 | 4 Pages |
Abstract
The reaction of 2-formylpyrrole acetals with sodium alkoxide in alcohols at reflux temperature smoothly proceeded to generate corresponding transacetalization products in nearly quantitative yields. A plausible mechanism involving the formation of a highly reactive intermediate azafulvene species was proposed to explain the observed transformation.
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Chemistry (General)
Authors
Zhao Hua Yan, Run Hua Kang, Yong Jie Liu, Sen Lin,