221035-77-4Relevant academic research and scientific papers
Design and synthesis of a s-triazene based asymmetric organocatalyst and its application in enantioselective alkylation
Mangawa, Shrawan K.,Singh, Ashawani K.,Awasthi, Satish K.
, p. 61144 - 61147 (2015/08/03)
A very efficient chiral organocatalyst was prepared from the readily available cyanuric chloride. The asymmetric catalyst exhibited a highly enantioselective catalytic performance for the alkylation of a glycinate Schiff base, which provides a useful procedure for the enantioselective synthesis of structurally diverse natural and unnatural α-alkyl-α-amino acids.
A convenient method for the enantiomeric separation of α-amino acid esters as benzophenone imine schiff base derivatives
Huang, Hu,Xu, Wen Jun,Jin, Jing-Yu,Hong, Joon Hee,Shin, Hyun-Jae,Lee, Wonjae
experimental part, p. 1015 - 1019 (2012/10/08)
A convenient liquid chromatographic method for the separation of α-amino acid esters as benzophenone Schiff base derivatives on coated chiral stationary phases (CSPs) (Chiralcel OD-H, Chiralcel OD, Chiralpak AD-H, Chiralpak AD, and Chiralpak AS) or covalently immobilized CSPs (Chiralpak IA, Chiralpak IB, and Chiralpak IC) derived from polysaccharide derivatives is described. Benzophenone imine derivatives of α-amino acid esters were readily prepared by stirring benzophenone imine and the hydrochloride salts of α-amino acid esters in 2-propanol. The chromatographic separations were conducted at a flow rate 1.0 mL/min and a detection wavelength of 254 nm; 0.5% 2-propanol/hexane (v/v) was used on CSPs. In general, the resolution of Chiralpak IC was superior to those of the other CSPs. In addition, the resolutions of other arylimine derivatives of α-amino acid esters and the effects of different mobile phases on the enantiomeric separation of α-amino acid esters as benzophenone imine derivatives on Chiralpak IC were investigated.
