ChemInform Abstract: A Versatile Catalyst for Reductive Amination by Transfer Hydrogenation.

ChemInform ◽  
2011 ◽  
Vol 42 (6) ◽  
pp. no-no
Author(s):  
Chao Wang ◽  
Alan Pettman ◽  
John Basca ◽  
Jianliang Xiao
Keyword(s):  
Reductive Amination ◽  
Transfer Hydrogenation

ChemInform Abstract: Direct Reductive Amination of Aromatic Aldehydes Catalyzed by Gold(I) Complex under Transfer Hydrogenation Conditions.

ChemInform ◽  
2011 ◽  
Vol 42 (42) ◽  
pp. no-no
Author(s):  
Ming Zhang ◽  
Hongwei Yang ◽  
Yan Zhang ◽  
Chengjian Zhu ◽  
Wei Li ◽  
...  
Keyword(s):  
Reductive Amination ◽  
Aromatic Aldehydes ◽  
Transfer Hydrogenation

A One-Pot Process for the Enantioselective Synthesis of Amines via Reductive Amination under Transfer Hydrogenation Conditions

2003 ◽  
Vol 5 (22) ◽  
pp. 4227-4230 ◽  
Author(s):  
Glynn D. Williams ◽  
Richard A. Pike ◽  
Charles E. Wade ◽  
Martin Wills
Keyword(s):  
Reductive Amination ◽  
Enantioselective Synthesis ◽  
Transfer Hydrogenation ◽  
One Pot

A Versatile Catalyst for Reductive Amination by Transfer Hydrogenation

2010 ◽  
Vol 122 (41) ◽  
pp. 7710-7714 ◽  
Author(s):  
Chao Wang ◽  
Alan Pettman ◽  
John Basca ◽  
Jianliang Xiao
Keyword(s):  
Reductive Amination ◽  
Transfer Hydrogenation

A Versatile Catalyst for Reductive Amination by Transfer Hydrogenation

2010 ◽  
Vol 49 (41) ◽  
pp. 7548-7552 ◽  
Author(s):  
Chao Wang ◽  
Alan Pettman ◽  
John Basca ◽  
Jianliang Xiao
Keyword(s):  
Reductive Amination ◽  
Transfer Hydrogenation

scholarly journals Base-Free Synthesis of Furfurylamines from Biomass Furans Using Ru Pincer Complexes

Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 558
Author(s):  
Danielle Pinheiro ◽  
Martin Nielsen
Keyword(s):  
Reductive Amination ◽  
Transfer Hydrogenation ◽  
Pincer Complexes

We report the first example of employing homogeneous organometal-catalyzed transfer hydrogenation for the selective reductive amination of furfurals to furfurylamines. An efficient, chemoselective, and base-free method is described using Ru-MACHO-BH as catalyst and iPrOH as H donor. The method tolerates a range of substituents affording moderate to excellent yields.

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