| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 68853 | Journal of Molecular Catalysis A: Chemical | 2007 | 5 Pages |
Abstract
The addition of acetanilides to ethyl propiolate proceeds under neutral conditions in the presence of triphenylphosphine to give the corresponding α-substituted alkyl acrylates together with variable amounts of the β-substituted isomer with (E) geometry. Addition of arylsulfonylanilides to alkyl propiolates under similar conditions, produced only the alkyl (E)-3-arylsulfonylanilino-2-propenoates.
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Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Issa Yavari, Norollah Hazeri, Malek T. Maghsoodlou, Sanaz Souri,