MICROWAVE-INDUCED BISMUTH NITRATE-CATALYZED EXPEDITIOUS ENAMINATION OF β-DICARBONYL COMPOUNDS UNDER SOLVENT-FREE CONDITIONS

Authors

Debasish Bandyopadhyay, The University of Texas Rio Grande ValleyFollow
Bimal K. Banik, The University of Texas Rio Grande Valley

Document Type

Article

Publication Date

2011

Abstract

Bismuth nitrate-catalyzed, automated microwave-assisted expeditious synthesis of β- enaminones and β-enaminoesters has been carried out in an efficient manner under solvent-free condition. The reaction is general for primary, secondary (cyclic, heterocyclic and acyclic), benzylic as well as aromatic amines.

Recommended Citation

Bandyopadhyay, D., & Banik, B. K. (2011). MICROWAVE-INDUCED BISMUTH NITRATE-CATALYZED EXPEDITIOUS ENAMINATION OF β-DICARBONYL COMPOUNDS UNDER SOLVENT-FREE CONDITIONS. Heterocyclic Letters, 1, 17–21.

First Page

17

Last Page

21

Publication Title

Heterocyclic Letters