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Kinetics of aminolysis for 1-thio-β- D-glucopyranosyl esters of N-acylalanines (CROSBI ID 163564)
Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija
Horvat, Štefica ; Tomić, Srđanka ; Jeričević, Željko
Kinetics of aminolysis for 1-thio-β- D-glucopyranosyl esters of N-acylalanines // Tetrahedron, 40 (1984), 6; 1047-1050. doi: 10.1016/S0040-4020(01)91244-X
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Horvat, Štefica ; Tomić, Srđanka ; Jeričević, Željko
engleski
Kinetics of aminolysis for 1-thio-β- D-glucopyranosyl esters of N-acylalanines
The kinetics of aminolysis of l-thio-β-D-glucopyranosyl esters of N-protected alanines (l) in dichloromethane, at 26°, by ethyl glycinate, under pseudo-first-order conditions follows the relationship kobsd=k2[H-Gly-(0Et].Significant differences were observed in the rates of dipeptide forming aminolysis for l-thiolesters la-lf, depending on N-acyl substituents and the configuration of alanine.
kinetics ; aminolysis ; glucopyranosyl esters
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