Catalyst-Dependent Selective Hydrogenation of Nitriles: Selective Synthesis of Tertiary and Secondary Amines

2017 ◽  
Vol 82 (20) ◽  
pp. 10939-10944 ◽  
Author(s):  
Yasunari Monguchi ◽  
Masahiro Mizuno ◽  
Tomohiro Ichikawa ◽  
Yuki Fujita ◽  
Eri Murakami ◽  
...  
2014 ◽  
Vol 50 (26) ◽  
pp. 3512-3515 ◽  
Author(s):  
Shuanglong Lu ◽  
Jiaqing Wang ◽  
Xueqin Cao ◽  
Xinming Li ◽  
Hongwei Gu

A series of both symmetrical and unsymmetrical secondary amines are synthesized from hydrogenation of nitriles under mild conditions.


2013 ◽  
Vol 2013 (18) ◽  
pp. 3671-3674 ◽  
Author(s):  
Svenja Werkmeister ◽  
Christoph Bornschein ◽  
Kathrin Junge ◽  
Matthias Beller

ChemInform ◽  
2013 ◽  
Vol 44 (45) ◽  
pp. no-no
Author(s):  
Svenja Werkmeister ◽  
Christoph Bornschein ◽  
Kathrin Junge ◽  
Matthias Beller

2015 ◽  
Vol 137 (28) ◽  
pp. 8888-8891 ◽  
Author(s):  
Arup Mukherjee ◽  
Dipankar Srimani ◽  
Subrata Chakraborty ◽  
Yehoshoa Ben-David ◽  
David Milstein

2007 ◽  
Vol 72 (4) ◽  
pp. 468-474 ◽  
Author(s):  
Peter T. Witte

Nitriles are converted to primary amines with high selectivity using a newly developed alumina-supported rhodium catalyst. The high selectivity is obtained without any additives, which are often used to prevent the formation of higher amines. The catalyst is active under mild conditions in various solvents, which makes it specifically suitable for use in pharmaceutical applications or for other substrates that can react with additives like strong acids or bases.


2016 ◽  
Vol 52 (9) ◽  
pp. 1812-1815 ◽  
Author(s):  
Subrata Chakraborty ◽  
Gregory Leitus ◽  
David Milstein

A novel complex based on earth-abundant iron, and its application in the catalytic homogeneous hydrogenation of (hetero)aromatic, benzylic, and aliphatic nitriles to selectively form primary amines is discovered.


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