The use of penicillin acylase for selective N-terminal deprotection in peptide synthesis
- 1 January 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (10) , 1131-1134
- https://doi.org/10.1016/s0040-4039(00)86668-x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Synthese von Glycopeptiden, Partialstrukturen biologischer ErkennungskomponentenAngewandte Chemie, 1987
- Immobilized benzylpenicillin acylase: Application to the synthesis of optically active forms of carnitin and propranalolTetrahedron Letters, 1986
- Immobilized penicillinacylase: Application to the synthesis of the dipeptide aspartameTetrahedron Letters, 1986
- Die Allylgruppe als mild und selektiv abspaltbare Carboxy-Schutzgruppe zur Synthese empfindlicherO-GlycopeptideAngewandte Chemie, 1984
- Approach to the use of benzylpenicillin acylase for configurational correlations of amino compounds. 2. Hydrolysis of N-(p-aminophenylacetyl) derivatives of some chiral primary aminesThe Journal of Organic Chemistry, 1979
- Approach to the use of benzylpenicillinacylase for configurational correlations of amino compoundsThe Journal of Organic Chemistry, 1978
- [54b] Penicillin acylase (bacterial)Published by Elsevier ,1975
- Eine neue Methode zur Synthese von Peptiden: Aktivierung der Carboxylgruppe mit Dicyclohexylcarbodiimid unter Zusatz von 1‐Hydroxy‐benzotriazolenEuropean Journal of Inorganic Chemistry, 1970
- New convenient reagent for peptide synthesesJournal of the American Chemical Society, 1968
- N-Acylaminosäuren IYAKUGAKU ZASSHI, 1965