Efficient and Mild Procedure for Reductive Methylation of Amines Using N??Methylpiperidine Zinc Borohydride
H Alinezhad, M Tajbakhsh, R Zamani
Index: Alinezhad, Heshmatollah; Tajbakhsh, Mahmood; Zamani, Reza Synthetic Communications, 2006 , vol. 36, # 23 p. 3609 - 3615
Full Text: HTML
Citation Number: 15
Abstract
Abstract A simple and efficient procedure for reductive methylation of primary and secondary amines using N??methylpiperidine zinc borohydride (ZBNMPP), giving tertiary amines, is described. The reaction is carried out in methanol at room temperature under neutral conditions.
Related Articles:
[Miura; Ootsuka; Suda; Nishikori; Hosomi Synlett, 2001 , # 10 p. 1617 - 1619]
[Tomashenko, Olesya; Sokolov, Viktor; Tomashevskiy, Alexander; Buchholz, Herwig A.; Welz-Biermann, Urs; Chaplinski, Vladimir; De Meijere, Armin European Journal of Organic Chemistry, 2008 , # 30 p. 5107 - 5111]
[Murai, Toshiaki; Matsushita, Koji Phosphorus, Sulfur and Silicon and the Related Elements, 2011 , vol. 186, # 5 p. 1094 - 1103]
[Journal of the American Chemical Society, , vol. 72, p. 2510,2514]
[Chemistry - A European Journal, , vol. 15, # 46 p. 12780 - 12790]