Asymmetric synthesis of threonine and retroracemization of amino acids using Ni(II) complexes of Schiff bases with S-2-n-(N?-benzylprolyl)aminobenzaldehyde

Author(s):  
Yu. N. Belokon' ◽  
N. I. Chernoglazova ◽  
K. A. Kochetkov ◽  
N. S. Garbalinskaya ◽  
M. G. Ryzhov ◽  
...  
ChemInform ◽  
2013 ◽  
Vol 44 (46) ◽  
pp. no-no
Author(s):  
Alexander E. Sorochinsky ◽  
Jose Luis Acena ◽  
Hiroki Moriwaki ◽  
Tatsunori Sato ◽  
Vadim A. Soloshonok

Molecules ◽  
2020 ◽  
Vol 25 (12) ◽  
pp. 2739 ◽  
Author(s):  
Yupiao Zou ◽  
Jianlin Han ◽  
Ashot S. Saghyan ◽  
Anna F. Mkrtchyan ◽  
Hiroyuki Konno ◽  
...  

Tailor-made amino acids are indispensable structural components of modern medicinal chemistry and drug design. Consequently, stereo-controlled preparation of amino acids is the area of high research activity. Over last decade, application of Ni(II) complexes of Schiff bases derived from glycine and chiral tridentate ligands has emerged as a leading methodology for the synthesis of various structural types of amino acids. This review article summarizes examples of asymmetric synthesis of tailor-made α-amino acids via the corresponding Ni(II) complexes, reported in the literature over the last four years. A general overview of this methodology is provided, with the emphasis given to practicality, scalability, cost-structure and recyclability of the chiral tridentate ligands.


Tetrahedron ◽  
1980 ◽  
Vol 36 (8) ◽  
pp. 1089-1097 ◽  
Author(s):  
Yu.N. Belokon ◽  
I.E. Zel'Tzer ◽  
N.M. Loim ◽  
V.A. Tsiryapkin ◽  
G.G. Aleksandrov ◽  
...  

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