A novel solid-phase linker strategy for the side-chain anchoring of arginine: an expeditious route to arginine 7-amido-4-methylcoumarins

Autor:	Joerg Beythien, Peter Schneeberger, Peter D. White, Sophie Barthélémy
Rok vydání:	2006
Předmět:	chemistry.chemical_classification Arginine Chemistry Organic Chemistry Anchoring Peptide Biochemistry Combinatorial chemistry chemistry.chemical_compound Phase (matter) Drug Discovery Side chain Peptide synthesis Linker
Zdroj:	Tetrahedron Letters. 47:3009-3012
ISSN:	0040-4039
Popis:	A novel linker strategy for the efficient side-chain anchoring of arginine is described. The utility of this approach was demonstrated by the facile synthesis of arginine-specific fluorogenic peptide substrates by standard Fmoc solid phase peptide synthesis methods.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::bee962435a1e1f67ecf2870f32bfac52 https://doi.org/10.1016/j.tetlet.2006.03.019 Zobrazit plný text záznamu Full Text from ScienceDirect