Enantioselective synthesis of episulfide analogues of L-methionine

Autor:	D. Guillerm, G. Guillerm
Rok vydání:	1992
Předmět:	Methionine Organic Chemistry Iodolactonization Enantioselective synthesis chemistry.chemical_element Iodine Biochemistry chemistry.chemical_compound chemistry Drug Discovery Organic chemistry Stereoselectivity Sodium thiocyanate Episulfide
Zdroj:	Tetrahedron Letters. 33:5047-5050
ISSN:	0040-4039
DOI:	10.1016/s0040-4039(00)61185-1
Popis:	Novel functionalized aminoacid analogues of L-methionine were prepared stereoselectively in three steps via iodolactonization of (S)-trans and (S)-cis crotylglycines.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::9566205547a2da54f043582d52fdafe7 https://doi.org/10.1016/s0040-4039(00)61185-1 Zobrazit plný text záznamu