Substrate Scope Evaluation of the Enantioselective Reduction of β-Alkyl-β-arylnitroalkenes by Old Yellow Enzymes 1-3 for Organic Synthesis Applications

ChemCatChem ◽  
2015 ◽  
Vol 8 (3) ◽  
pp. 577-583 ◽  
Author(s):  
Mattia Bertolotti ◽  
Elisabetta Brenna ◽  
Michele Crotti ◽  
Francesco G. Gatti ◽  
Daniela Monti ◽  
...  
Keyword(s):  
Organic Synthesis ◽  
Enantioselective Reduction

Enantioselective imine reduction catalyzed by imine reductases and artificial metalloenzymes

2014 ◽  
Vol 12 (19) ◽  
pp. 2989-2992 ◽  
Author(s):  
Daniela Gamenara ◽  
Pablo Domínguez de María
Keyword(s):  
Organic Synthesis ◽  
Chiral Amines ◽  
Enantioselective Reduction ◽  
Artificial Metalloenzymes ◽  
Imine Reduction

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.

Lithiated γ-Tosyl-Substituted Benzylmethallylamine:  New γ-Amino Methallyl Sulfone Anions in Organic Synthesis

1997 ◽  
Vol 62 (5) ◽  
pp. 1564-1564
Author(s):  
Diego A. Alonso ◽  
Larry R. Falvello ◽  
Balbino Mancheño ◽  
Carmen Nájera ◽  
Milagros Tomás
Keyword(s):  
Organic Synthesis
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