ChemInform Abstract: Reductive Amination/Cyclization of Keto Acids Using a Hydrosilane for Selective Production of Lactams versus Cyclic Amines by Switching of the Indium Catalyst.

ChemInform ◽  
2016 ◽  
Vol 47 (23) ◽  
Author(s):  
Yohei Ogiwara ◽  
Takuya Uchiyama ◽  
Norio Sakai
2018 ◽  
Vol 8 (19) ◽  
pp. 4994-5002 ◽  
Author(s):  
Xinkuan Cheng ◽  
Xi Chen ◽  
Jinhui Feng ◽  
Qiaqing Wu ◽  
Dunming Zhu

Structure-guided reshaping the substrate-binding pocket of ameso-diaminopimelate dehydrogenase (StDAPDH) led to a mutant W121L/H227I, which catalyzed the enantioselective reductive amination of some sterically bulky 2-keto acids.


1978 ◽  
Vol 31 (1) ◽  
pp. 73 ◽  
Author(s):  
EA Jeffery ◽  
A Meisters

Racemic 2-amino-2-phenylacetic acid, monoammonium glutamate, 2-aminobutyric acid, α-alanine and ammonium 5-amino-5-phenylvalerate have been prepared by electrochemical reductive amination of the corresponding keto acids in aqueous ammonia/ammonium chloride solution at a mercury electrode. The yields ranged from 24% for ammonium 5-amino-5-phenylvalerate to 88% for 2-amino-2-phenylacetic acid. The current efficiency and yield of 2-amino-2-phenylacetic acid from reductive amination of 2-oxo-2-phenylacetic acid increased with increase in ammonia concentration. Also, decreasing the reduction potential from -1.10 to -1.30 V (with respect to a saturated calomel electrode) in 2 M ammonia raised the initial current density from c. 2 mA/cm2 to c. 7 mA/cm2 but halved the yield of 2-amino-2-phenylacetic acid.


2017 ◽  
Vol 19 (16) ◽  
pp. 4215-4218 ◽  
Author(s):  
Ying Zhang ◽  
Qiaozhi Yan ◽  
Guofu Zi ◽  
Guohua Hou

2012 ◽  
pp. 1165-1203 ◽  
Author(s):  
Werner Hummel ◽  
Harald Gröger

2020 ◽  
Vol 22 (7) ◽  
pp. 2707-2713 ◽  
Author(s):  
Yongjie Shi ◽  
Xuefeng Tan ◽  
Shuang Gao ◽  
Yao Zhang ◽  
Jingxin Wang ◽  
...  

ACS Catalysis ◽  
2017 ◽  
Vol 7 (11) ◽  
pp. 7772-7776 ◽  
Author(s):  
Cailing Wu ◽  
Hongye Zhang ◽  
Bo Yu ◽  
Yu Chen ◽  
Zhengang Ke ◽  
...  

1955 ◽  
Vol 33 (1) ◽  
pp. 307-316 ◽  
Author(s):  
John K. Pollak ◽  
Donald Fairbairn

Homogenates of ascaris ovaries contained transamination, deamination, and reductive amination systems. Alanine–glutamic and aspartic–glutamic transaminases were active, whereas weaker transaminations occurred between glycine or serine and α-ketoglutaric or pyruvic acids. Sixteen other amino acids did not participate in transamination with these keto acids. A minor reaction, however, occurred between alanine or glutamic acid and α-ketovaleric acid. No amino acid oxidase activity was detected, and deamination appeared to be limited to a weakly positive glutamic dehydrogenase, which could be coupled to the alanine–glutamic and aspartic–glutamic transaminases to form a transdeaminase system. In the presence of pyruvate and ammonium chloride reductive amination occurred and alanine and aspartic acid were synthesized. This reaction was accelerated by bicarbonate, although oxalacetate could not be substituted successfully for pyruvate in the amination system. The results of the investigation are in accord with the probability that an active protein synthesis occurs in ascaris ovaries.


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