ChemInform Abstract: Asymmetric Synthesis of α-Amino Acids via Homologation of Ni(II) Complexes of Glycine Schiff Bases. Part 2. Aldol, Mannich Addition Reactions, Deracemization and (S) to (R) Interconversion of α-Amino Acids

ChemInform ◽  
2013 ◽  
Vol 44 (51) ◽  
pp. no-no
Author(s):  
Alexander E. Sorochinsky ◽  
Jose Luis Acena ◽  
Hiroki Moriwaki ◽  
Tatsunori Sato ◽  
Vadim Soloshonok
ChemInform ◽  
2013 ◽  
Vol 44 (46) ◽  
pp. no-no
Author(s):  
Alexander E. Sorochinsky ◽  
Jose Luis Acena ◽  
Hiroki Moriwaki ◽  
Tatsunori Sato ◽  
Vadim A. Soloshonok

Author(s):  
Yu. N. Belokon' ◽  
N. I. Chernoglazova ◽  
K. A. Kochetkov ◽  
N. S. Garbalinskaya ◽  
M. G. Ryzhov ◽  
...  

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.


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