Stereoselective Synthesis of Quaternary Proline Analogues

Autor:	Carlos Cativiela, M. Isabel Calaza
Rok vydání:	2008
Předmět:	Stereochemistry Organic Chemistry Enantioselective synthesis Combinatorial chemistry Article Pyrrolidine chemistry.chemical_compound chemistry Enantio selectivity Moiety Stereoselectivity Proline Physical and Theoretical Chemistry Quaternary
Zdroj:	European Journal of Organic Chemistry. 2008:3427-3448
ISSN:	1099-0690 1434-193X
DOI:	10.1002/ejoc.200800225
Popis:	This review describes available methods for the diastereoselective and asymmetric synthesis of quaternary prolines. The focus is on the preparation of alpha-functionalized prolines with the pyrrolidine moiety not embedded in a polycyclic frame. The diverse synthetic approaches are classified according to the bond which is formed to complete the quaternary skeleton.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2080af997fccf10c1eb0388d9fd59cac https://doi.org/10.1002/ejoc.200800225 Zobrazit plný text záznamu Plný text