Samarium Diiodide Catalyzed Aza-Michael Reactions for the Formation of β-Amino Amides

Author(s): Irena Reboule, Sophie Bezzenine-Lafollee, Jacqueline Collin, Richard Gil, Myriam Martin.

Journal Name: Letters in Organic Chemistry

Volume 7 , Issue 2 , 2010

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Abstract:

Samarium diiodide is an efficient Lewis acid type catalyst for the 1,4-addition of aromatic amines onto α,β- unsaturated N-benzoyl amides affording new β-amino amides. These reactions are compared with similar aza-Michael additions involving α,β-unsaturated-N-acyloxazolidinones.

Keywords: Samarium diiodide, catalysis, amines, Aza-Michael reaction, carbon-nitrogen bond formation

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Article Details

VOLUME: 7
ISSUE: 2
Year: 2010
Page: [94 - 97]
Pages: 4
DOI: 10.2174/157017810790796255
Price: $58

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