Broadening of the substrate tolerance of α-chymotrypsin by using the carbamoylmethyl ester as an acyl donor in kinetically controlled peptide synthesis

2001 ◽  
pp. 87-94 ◽  
Author(s):  
Toshifumi Miyazawa ◽  
Kayoko Tanaka ◽  
Eiichi Ensatsu ◽  
Ryoji Yanagihara ◽  
Takashi Yamada
Keyword(s):  
Peptide Synthesis ◽  
Acyl Donor ◽  
Kinetically Controlled ◽  
Carbamoylmethyl Ester ◽  
Substrate Tolerance

ChemInform Abstract: Superiority of the Carbamoylmethyl Ester as an Acyl Donor for the Kinetically Controlled Amide-Bond Formation Mediated by α-Chymotrypsin.

ChemInform ◽  
2010 ◽  
Vol 33 (25) ◽  
pp. no-no
Author(s):  
Toshifumi Miyazawa ◽  
Eiichi Ensatsu ◽  
Nobuhiro Yabuuchi ◽  
Ryoji Yanagihara ◽  
Takashi Yamada
Keyword(s):  
Bond Formation ◽  
Amide Bond ◽  
Acyl Donor ◽  
Amide Bond Formation ◽  
Kinetically Controlled ◽  
Carbamoylmethyl Ester

ChemInform Abstract: Protease-Catalyzed Kinetically Controlled Peptide Synthesis

ChemInform ◽  
2010 ◽  
Vol 23 (6) ◽  
pp. no-no
Author(s):  
V. SCHELLENBERGER ◽  
H.-D. JAKUBKE
Keyword(s):  
Peptide Synthesis ◽  
Kinetically Controlled

How to predict product yield in kinetically controlled enzymatic peptide synthesis

1992 ◽  
Vol 40 (3) ◽  
pp. 432-436 ◽  
Author(s):  
Mikhail Yu. Gololobov ◽  
Elena V. Kozlova ◽  
Ivan L. Borisov ◽  
Ute Schellenberger ◽  
Volker Schellenberger ◽  
...  
Keyword(s):  
Peptide Synthesis ◽  
Product Yield ◽  
Enzymatic Peptide Synthesis ◽  
Kinetically Controlled
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