Synthesis of Alkyl and Aryl Esters of N-Protected β-Homoamino Acids from N-Protected α-Aminodiazoketones

Autor:	Hosahudya N. Gopi, Ganga-Ramu Vasanthakumar, V V Suresh Babu
Rok vydání:	2002
Předmět:	chemistry.chemical_classification chemistry.chemical_compound chemistry Structural Biology Aryl Yield (chemistry) Organic chemistry Wolff rearrangement General Medicine Biochemistry Alkyl
Zdroj:	Protein & Peptide Letters. 9:529-532
ISSN:	0929-8665
Popis:	A simple and concomitant esterification method for the synthesis of methyl, ethyl, t-butyl, benzyl, and 9-fluorenylmethyl esters of Fmoc-/Boc-/Z-beta-homoamino acids employing Fmoc-/Boc-/Z-alpha-aminodiazoketones by Wolff rearrangement is described. The method offers good yield with purity.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::7129e670074bf3f5b4ea81927a7966bc https://doi.org/10.2174/0929866023408364 Zobrazit plný text záznamu