Phenylglycine racemization in Fmoc-based solid-phase peptide synthesis: Stereochemical stability is achieved by choice of reaction conditions-Reference-Cited by-同舟云学术

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Phenylglycine racemization in Fmoc-based solid-phase peptide synthesis: Stereochemical stability is achieved by choice of reaction conditions

Published:2017-06 Issue:24 Volume:58 Page:2325-2329
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Liang Chen,Behnam Mira A.M.,Sundermann Tom R.,Klein Christian D.

Funder

German Academic Exchange Service

Deutsche Forschungsgemeinschaft

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference26 articles.

1. Structural aspects of phenylglycines, their biosynthesis and occurrence in peptide natural products

2. Phenylglycine as a novel P2 scaffold in hepatitis C virus NS3 protease inhibitors

3. Improved P2 phenylglycine-based hepatitis C virus NS3 protease inhibitors with alkenylic prime-side substituents

4. P2–P1′ macrocyclization of P2 phenylglycine based HCV NS3 protease inhibitors using ring-closing metathesis

5. Dual inhibitors of the dengue and West Nile virus NS2B–NS3 proteases: Synthesis, biological evaluation and docking studies of novel peptide-hybrids

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