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
2019 ◽  
Vol 10 (8) ◽  
pp. 2473-2477 ◽  
Author(s):  
Tao Yang ◽  
Xiaochong Guo ◽  
Qin Yin ◽  
Xumu Zhang

An enantioselective synthesis of dibenz[c,e]azepines containing both central and axial chiralities through a one pot N-Boc deprotection/intramolecular asymmetric reductive amination sequence has been achieved with generally excellent enantiocontrol (up to 97% ee).


2018 ◽  
Vol 54 (52) ◽  
pp. 7247-7250 ◽  
Author(s):  
Tao Yang ◽  
Qin Yin ◽  
Guoxian Gu ◽  
Xumu Zhang

Asymmetric reductive amination for the synthesis of both chiral tetrahydroquinolines and tetrahydroisoquinolines has been realized with an Ir/ZhaoPhos catalytic system via a one-pot N-Boc deprotection/intramolecular asymmetric reductive amination (ARA) sequence.


Synthesis ◽  
2020 ◽  
Author(s):  
Yanping Xia ◽  
Lu Ouyang ◽  
Jianhua Liao ◽  
Xiao Yang ◽  
Renshi Luo

Hydrogenation of C=C bond and reductive amination is important transformation utilized in chemistry. An efficient and facile one-pot transfer hydrogenation of C=C bond and reductive amination of C=N bond of enones and amines was reported using the iridium complexes as catalysts and formic acid as hydrogen source in aqueous medium, which shows environmentally friendly. In this catalytic system, a wide range of α-alkylated amine compounds were obtained in excellent yields by one-pot transfer hydrogenation of C=C bond and reductive amination. The practical application of this protocol is characterized by gram-scale transformation.


Synthesis ◽  
2019 ◽  
Vol 51 (13) ◽  
pp. 2713-2719
Author(s):  
Huan Zhou ◽  
Wenlei Zhao ◽  
Tao Zhang ◽  
Haodong Guo ◽  
Haizhou Huang ◽  
...  

Catalyzed by the complex generated in situ from iridium and the chiral ferrocene ligand, tert-butyl (4-oxo-4-arylbutyl)carbamate substrates were deprotected and then reductively cyclised to form 2-substituted arylpyrrolidines in a one-pot manner, in which the intramolecular reductive amination was the key step. A range of chiral 2-substituted arylpyrrolidines were synthesised in up to 98% yield and 92% ee.


Author(s):  
Bolla Srinivasarao ◽  
Yogita Y ◽  
Dhana Lakshmi Darsi ◽  
Krishna Kumari Pamula ◽  
N. Lingaiah

One pot conversion of furfural to -valerolactone by transfer hydrogenation has been achieved over bifunctional Zr and TPA located in mesoporous silica catalysts. Different catalysts with TPA and ZrO2 located...


Author(s):  
Ruixia Liu ◽  
Jingkuo Han ◽  
Bin Li ◽  
Xian Liu ◽  
Zhao Wei ◽  
...  

A highly efficient intramolecular asymmetric reductive amination transformation catalyzed by an iridium complex of tBu-ax-Josiphos has been realized, providing an efficient access to various THIQ alkaloids.


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