Synthesis of a hydroxyethylene isostere of the tripeptide Arg-Gly-Leu via a convergent acyl-like radical addition strategy

Autor:	Jensen, C.M., Lindsay, K.B., Andreasen, P., Skrydstrup, T.
Jazyk:	angličtina
Rok vydání:	2005
Zdroj:	Jensen, C M, Lindsay, K D, Andreasen, P & Skrydstrup, T 2005, ' Synthesis of a hydroxyethylene isostere of the tripeptide Arg-Gly-Leu via a convergent acyl-like radical addition strategy ', J. Org. Chem., vol. 70, pp. 7512-7519 . Jensen, C M, Lindsay, K B, Andreasen, P & Skrydstrup, T 2005, ' Synthesis of a Hydroxyethylene Isostere of the Tripeptide Arg-Gly-Leu via a Convergent Acyl-like Radical Addition Strategy ', J. Org. Chem., vol. 70, pp. 7512-7519 .
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::42983332aeff61951ee47fe6f08d6111 https://pure.au.dk/portal/da/publications/synthesis-of-a-hydroxyethylene-isostere-of-the-tripeptide-argglyleu-via-a-convergent-acyllike-radical-addition-strategy(0f351280-ba74-11da-bee9-02004c4f4f50).html Zobrazit plný text záznamu