Prostanoids: Synthesis of Enantiomers of 15-Deoxy-16-hydroxy-16-methylprostaglandin E1

Autor:	Miroslav Terinek, Václav Kozmík, Jaroslav Paleček
Rok vydání:	1997
Předmět:	chemistry.chemical_classification chemistry Stereochemistry 15-deoxy-16-hydroxy-16-methylprostaglandin E1 General Chemistry Enantiomer Lactone
Zdroj:	Collection of Czechoslovak Chemical Communications. 62:1325-1341
ISSN:	1212-6950 0010-0765
DOI:	10.1135/cccc19971325
Popis:	Four optically pure isomers of methyl 11,16-dihydroxy-16-methyl-9-oxoprost-13-enoate (1a-1d) were synthesized using an approach reverse to the classical Corey procedure, the key intermediates being the easily accessible (-)- and (+)-enantiomers of the Corey lactone, 2a and 2b.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::cba4e916b143fc4133359e6b3f8b6061 https://doi.org/10.1135/cccc19971325 Zobrazit plný text záznamu