Peptide SynthesisviaAmino Acid Active Esters. II.1Some Abnormal Reactions during Peptide Synthesis

1962 ◽  
Vol 84 (7) ◽  
pp. 1279-1283 ◽  
Author(s):  
Murray. Goodman ◽  
Kenneth C. Stueben
1988 ◽  
Vol 53 (1) ◽  
pp. 145-156 ◽  
Author(s):  
Jana Pírková ◽  
Svetlana Churkina ◽  
Vladimír Gut ◽  
Ivo Frič ◽  
Karel Bláha

The sequential polypeptides (Lys-Ala)n, (Lys-Ala-Ala)n, (Lys-Ala-Ala-Ala)n, (Lys-Leu-Ala)n, (Lys-Leu-Ala-Ala)n, (Lys-Leu-Ala-Ala-Ala)n, (Lys-Ala-Leu)n, (Lys-Ala-Leu-Ala)n, (Orn-Leu-Ala)n,(Arg-Ala-Ala)n, (Arg-Leu-Ala)n, (Arg-Leu-Ala-Ala)n, (Arg-Ala-Leu)n, and (Arg-Ala-Leu-Ala)n were synthesized by polymerization of active esters (1-succinimidyl or pentafluorophenyl) of the corresponding Nα-deblocked monomers. The monomers were prepared using the usual methods of peptide synthesis in solution. Upon dialysis, the average molecular weight of the polymer was 6 000-9 000 as determined by sedimentation in ultracentrifuge. Polypeptides, containing leucine in addition to the basic amino acid, showed a marked tendency to aggregation. CD spectra of the products were measured for characterization.


1974 ◽  
Vol 5 (24) ◽  
pp. no-no
Author(s):  
MIKLOS BODANSZKY ◽  
MARY LYNN FINK ◽  
KENNETH W. FUNK ◽  
MICHIO KONDO ◽  
CYNTHIA YANG LIN ◽  
...  

1989 ◽  
Vol 8 (4) ◽  
pp. 461-469 ◽  
Author(s):  
Miklos Bodanszky ◽  
Maria A. Bednarek

1974 ◽  
Vol 5 (49) ◽  
pp. no-no
Author(s):  
M. FUJINO ◽  
S. KOBAYASHI ◽  
M. OBAYASHI ◽  
T. FUKUDA ◽  
S. SHINAGAWA ◽  
...  

1964 ◽  
Vol 17 (11) ◽  
pp. 1282 ◽  
Author(s):  
B Halpern ◽  
LB James

The reaction of dimedone (5,5-dimethylcyclohexane-1,3-dione) with amino-acid "active" esters leads to optically pure enamine derivatives. The dimedone derivatives of amino acid esters could also be converted by way of their hydrazides to the corresponding azides. The thiophenyl ester and azide derivatives have been used directly for peptide synthesis. The protecting group can easily be removed from the N-protected peptides by means of aqueous bromine, with the formation of 2,2-dibromodimedone and the hydrobromide of the corresponding peptide ester.


1975 ◽  
Vol 6 (4) ◽  
pp. no-no
Author(s):  
PAOLO GIORI ◽  
MARIO GUARNERI ◽  
DIONISIO MAZZOTTA ◽  
CARLO ALBERTO BENASSI

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