LiClO 4 accelerated Michael addition of amines to α, β-unsaturated olefins under solvent-free conditions
N Azizi, MR Saidi
Index: Azizi, Najmedin; Saidi, Mohammad R. Tetrahedron, 2004 , vol. 60, # 2 p. 383 - 387
Full Text: HTML
Citation Number: 179
Abstract
Recently, LiClO 4 has emerged as a powerful promoter in many chemical processes and in different organic media. 5 In this context, it is worthy to note that, due to the remarkable tolerance of LiClO 4 toward coordinating functional groups, even strongly coordinating amines can be used in the presence of LiClO 4 . 6 We have taken advantage of this compatibility in developing a practical, simple and environmentally benign methodology for the conjugate addition of ...
Related Articles:
[Tanaka, Yusuke; Hasui, Tomoaki; Suginome, Michinori Synlett, 2008 , # 8 p. 1239 - 1242]
The addition of saturated heterocyclic amines to cinnamate esters
[Pollard; Mattson Journal of the American Chemical Society, 1956 , vol. 78, p. 4089]
Synthesis and CNS Activity of New 3??Amino??3??arylpropionic Acid Derivatives
[Renault; Guillon; Huard; Miel; Stiebing; Le Bourn; Boulouard; Dallemagne; Rault Pharmacy and Pharmacology Communications, 1999 , vol. 5, # 3 p. 217 - 223]
Synthesis and CNS Activity of New 3??Amino??3??arylpropionic Acid Derivatives
[Renault; Guillon; Huard; Miel; Stiebing; Le Bourn; Boulouard; Dallemagne; Rault Pharmacy and Pharmacology Communications, 1999 , vol. 5, # 3 p. 217 - 223]
Synthesis and CNS Activity of New 3??Amino??3??arylpropionic Acid Derivatives
[Renault; Guillon; Huard; Miel; Stiebing; Le Bourn; Boulouard; Dallemagne; Rault Pharmacy and Pharmacology Communications, 1999 , vol. 5, # 3 p. 217 - 223]