Use of 2,4,6 - tribromophenyl, aminoacid esters in peptide synthesis
β Scribed by T. Scott-Burden; A.O. Hawtrey
- Publisher
- Elsevier Science
- Year
- 1967
- Tongue
- French
- Weight
- 110 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0040-4039
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π SIMILAR VOLUMES
The ability of the endopeptidase a-chymotrypsin (EC 3.4.21.1) to catalyse the reaction of various N aunprotected di-and tripeptide ester derivatives with H-Leu-NH 2 , and with a series of C-terminal free di-and tripeptides at ΓΏ15 C in frozen aqueous solution was investigated. The enzyme is able to s
Practical procedures have been developed for synthesis of peptides using lipases and esterases as catalysts. We describe here a new strategy for enzymatic peptide synthesis using an esterase without amidase activity as a catalyst and N-acyl amino acid esters and amino acid esters as substrates in e