Autor:	Stephen G. Davies, Jeffrey Mckenna, Charles J. R. Hedgecock
Rok vydání:	1995
Předmět:	Inorganic Chemistry chemistry.chemical_compound Thienamycin Lithium amide chemistry Stereochemistry Organic Chemistry Michael reaction Enantioselective synthesis Physical and Theoretical Chemistry Catalysis Sequence (medicine)
Zdroj:	Tetrahedron: Asymmetry. 6:2507-2510
ISSN:	0957-4166
DOI:	10.1016/0957-4166(95)00327-l
Popis:	Synthesis of an enantiomerically pure intermediate to (+)-thienamycin is presented: the pivotal reaction in this sequence is the highly diastereoselective Michael addition of a differentially protected lithium amide.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da63365a8aeae8a25d53b03f5acd98d3 https://doi.org/10.1016/0957-4166(95)00327-l Zobrazit plný text záznamu Full Text from ScienceDirect