A general and selective copper-catalyzed reduction of secondary amides
S Das, B Join, K Junge, M Beller
Index: Das, Shoubhik; Join, Benoit; Junge, Kathrin; Beller, Matthias Chemical Communications, 2012 , vol. 48, # 21 p. 2683 - 2685
Full Text: HTML
Citation Number: 36
Abstract
Reduction of amides constitutes an important synthetic method for the preparation of functionalized amines both on the laboratory as well as on the industrial scale. Until today, often traditional boron and aluminium hydride-mediated reductions prevail for such processes. 1 Tedious product purification and concomitant formation of salt by-products are disadvantages of these stoichiometric procedures. In contrast, catalytic methods offer more versatile strategies for selective ...
Related Articles:
Reductive Amination of Aldehydes and Amines with an Efficient Pd/NiO Catalyst
[Yang, Huimin; Cui, Xinjiang; Deng, Youquan; Shi, Feng Synthetic Communications, 2014 , vol. 44, # 9 p. 1314 - 1322]
Reductive amination of aromatic aldehydes and ketones with nickel boride
[Saxena, Ira; Borah, Ruli; Sarma, Jadab C. Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 4 p. 503 - 504]
[Cui, Xinjiang; Dai, Xingchao; Deng, Youquan; Shi, Feng Chemistry - A European Journal, 2013 , vol. 19, # 11 p. 3665 - 3675]
[Ranu, Brindaban C.; Sarkar, Arunkanti; Majee, Adinath Journal of Organic Chemistry, 1997 , vol. 62, # 6 p. 1841 - 1842]
[Fujita, Ken-ichi; Enoki, Youichiro; Yamaguchi, Ryohei Tetrahedron, 2008 , vol. 64, # 8 p. 1943 - 1954]