HBF 4· OEt 2 as a mild and versatile reagent for the Ritter amidation of olefins: a facile synthesis of secondary amides
BVS Reddy, NS Reddy, C Madan, JS Yadav
Index: Subba Reddy; Sivasankar Reddy; Madan, Ch.; Yadav Tetrahedron Letters, 2010 , vol. 51, # 37 p. 4827 - 4829
Full Text: HTML
Citation Number: 26
Abstract
A variety of alkenes undergo smooth amidation with nitriles in the presence of HBF4· OEt2 at room temperature under mild conditions to afford the corresponding secondary amides in good to excellent yields. This is a highly efficient method for the preparation of α-aryl ethyl amides especially from vinyl arenes without any side reactions such as olefin polymerization. The use of readily available and easy to handle reagent HBF4· OEt2 ...
Related Articles:
[Chazalette, Celine; Masereel, Bernard; Rolin, Stephanie; Thiry, Anne; Scozzafava, Andrea; Innocenti, Alessio; Supuran, Claudiu T. Bioorganic and Medicinal Chemistry Letters, 2004 , vol. 14, # 23 p. 5781 - 5786]
[Nair, Vijay; Suja; Mohanan, Kishor Tetrahedron Letters, 2005 , vol. 46, # 18 p. 3217 - 3219]
Enantioselective acylation of chiral amines catalysed by aminoacylase I
[Youshko, Maxim I; Van Rantwijk, Fred; Sheldon, Roger A Tetrahedron Asymmetry, 2001 , vol. 12, # 23 p. 3267 - 3271]
Enantioselective acylation of chiral amines catalysed by aminoacylase I
[Youshko, Maxim I; Van Rantwijk, Fred; Sheldon, Roger A Tetrahedron Asymmetry, 2001 , vol. 12, # 23 p. 3267 - 3271]