Use of phenylacetyl group for protection of the lysine Nε-amino group in synthesis of peptides-Reference-Cited by-同舟云学术

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Use of phenylacetyl group for protection of the lysine Nε-amino group in synthesis of peptides

Published:1981 Issue:8 Volume:46 Page:1983-1989
ISSN:0010-0765
Container-title:Collection of Czechoslovak Chemical Communications
language:en
Short-container-title:Collect. Czech. Chem. Commun.

Author:

Brtník František,Barth Tomislav,Jošt Karel

Abstract

Nε-Phenylacetyllysine was used in the synthesis of deamino-lysine-vasopressin. The phenylacetyl protecting group is stable under conditions of peptide synthesis and can be removed by action of penicillin amidohydrolase (E.C.3.5.1.11) without damaging the built peptide chain.

Publisher

Institute of Organic Chemistry & Biochemistry

Subject

General Chemistry

Cited by 21 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A chemoenzymatic strategy for site-selective functionalization of native peptides and proteins;Science;2022-06-17

2. Metal Complexes of Biologically Important Ligands, CLXXII [1]. Metal Ions and Metal Complexes as Protective Groups of Amino Acids and Peptides – Reactions at Coordinated Amino Acids;Zeitschrift für Naturforschung B;2009-12-01

3. The use of Fmoc-Lys(Pac)-OH and penicillin G acylase in the preparation of novel semisynthetic insulin analogs;Journal of Peptide Science;2007

4. Enzymatic Protecting Group Techniques;Chemical Reviews;2001-09-20

5. N-Protection of Amino Acid Derivatives Catalyzed by Immobilized Penicillin G Acylase;Biocatalysis and Biotransformation;1996-01

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