Title of article
Aza-Michael reactions catalyzed by samarium diiodide
Author/Authors
Reboule، نويسنده , , Iréna and Gil، نويسنده , , Richard and Collin، نويسنده , , Jacqueline، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
4
From page
7761
To page
7764
Abstract
Samarium diiodide catalyzes the Michael addition of aromatic amines onto α,β-unsaturated N-acyloxazolidinones to form β-aminoacid derivatives. Aza-Michael reactions can be followed by an amidation reaction with the aromatic amine, leading to β-aminoamides. β-Amino-N-acyloxazolidinones are selectively obtained with o-anisidine, while amidation reaction is observed with p-anisidine.
Keywords
Samarium diiodide , Amines , Catalysis , Aza-Michael reaction , Carbon–nitrogen bond formation
Journal title
Tetrahedron Letters
Serial Year
2005
Journal title
Tetrahedron Letters
Record number
1847214
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