ChemInform Abstract: Enantioselective Imine Reduction Catalyzed by Imine Reductases and Artificial Metalloenzymes

ChemInform ◽  
2014 ◽  
Vol 45 (27) ◽  
pp. no-no
Author(s):  
Daniela Gamenara ◽  
Pablo Dominguez de Maria
2014 ◽  
Vol 12 (19) ◽  
pp. 2989-2992 ◽  
Author(s):  
Daniela Gamenara ◽  
Pablo Domínguez de María

Adding value to organic synthesis. Novel imine reductases enable the enantioselective reduction of imines to afford chiral amines. Likewise, novel bioinspired artificial metalloenzymes can perform the same reaction as well. Remarkable recent examples are herein discussed.


2019 ◽  
Vol 21 (42) ◽  
pp. 23408-23417 ◽  
Author(s):  
Haisong Feng ◽  
Xuan Guo ◽  
Hui Zhang ◽  
Lifang Chen ◽  
Pan Yin ◽  
...  

The anchoring effect of artificial metalloenzymes determines the chirality of the product of imine reduction.


RSC Advances ◽  
2021 ◽  
Vol 11 (34) ◽  
pp. 20961-20969
Author(s):  
Yunqing He ◽  
Wanli Nie ◽  
Ying Xue ◽  
Qishan Hu

Hydrosilylation or amination products? It depends on water amount and nucleophiles like excess water or produced/added amines.


2021 ◽  
pp. 177-205
Author(s):  
Kevin A. Harnden ◽  
Yajie Wang ◽  
Lam Vo ◽  
Huimin Zhao ◽  
Yi Lu

Author(s):  
Shreyans Chordia ◽  
Siddarth Narasimhan ◽  
Alessandra Lucini Paioni ◽  
Marc Baldus ◽  
Gerard Roelfes

2020 ◽  
Vol 1 (5) ◽  
pp. 369-378
Author(s):  
Rosalind L. Booth ◽  
Gideon Grogan ◽  
Keith S. Wilson ◽  
Anne-Kathrin Duhme-Klair

This review surveys the development of this class of artificial metalloenzymes and provides a perspective on existing and future research in the area.


2019 ◽  
Vol 7 ◽  
Author(s):  
Tatjana N. Parac-Vogt ◽  
Andrea Erxleben ◽  
Gerhard Schenk ◽  
Rajeev Prabhakar

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