Synthesis of homo-and heterobiarylmethylamines
V Terrasson, S Marque, A Scarpacci, D Prim
Index: Terrasson, Vincent; Marque, Sylvain; Scarpacci, Annabelle; Prim, Damien Synthesis, 2006 , # 11 p. 1858 - 1862
Full Text: HTML
Citation Number: 7
Abstract
We first investigated the preparation of symmetric targets (Scheme [1] : Ar 1 = Ar 2 , Table [1] ). In the case of diphenylmethylamine 1, several nucleophiles (Li, Mg, Cu) have been tested. [10] The best combination, involving phenylmagnesium chloride and benzonitrile in THF, afforded the expected compound in 64 to 73% yields. The amines were easily purified by careful acidic-basic treatment of the crude material. Arylmagnesium chlorides have been ...
Related Articles:
[Yu, Ming; Tang, Ri-Yuan; Li, Jin-Heng Tetrahedron, 2009 , vol. 65, # 17 p. 3409 - 3416]
[Burns, Michael J.; Fairlamb, Ian J. S.; Kapdi, Anant R.; Sehnal, Petr; Taylor, Richard J. K. Organic Letters, 2007 , vol. 9, # 26 p. 5397 - 5400]
[Uozumi, Yasuhiro; Nakai, Yasushi Organic Letters, 2002 , vol. 4, # 17 p. 2997 - 3000]
[Buzhansky, Ludmila; Feit, Ben-Ami Journal of Organic Chemistry, 2002 , vol. 67, # 21 p. 7523 - 7525]
[Parrish, Jay P.; Flanders, Vincent L.; Floyd, Ryan J.; Jung, Kyung Woon Tetrahedron Letters, 2001 , vol. 42, # 44 p. 7729 - 7731]