Methods for obtaining optically active intermediates for prostaglandin synthesis [review]

Autor:	V. L. Khristoforov, V. A. Serebryanyi
Rok vydání:	1994
Předmět:	Pharmacology chemistry.chemical_compound chemistry Drug Discovery Pharmacology toxicology Prostaglandin synthesis Enantioselective synthesis Prostaglandin Organic chemistry Optically active
Zdroj:	Pharmaceutical Chemistry Journal. 28:412-440
ISSN:	1573-9031 0091-150X
DOI:	10.1007/bf02285402
Popis:	Thus, obtaining chiral precursors of prostaglandins has been described in the literature using most of the familiar enantioselective synthesis methods. At the same time, the large number of the techniques used makes it possible to draw the conclusion that there is no single universal method for obtaining enantiomerically pure prostaglandin intermediates. Therefore the search for new approaches to obtaining optically active intermediates for prostaglandin synthesis remains timely even today.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::318c463b308087fd5786912e4cd92bb7 https://doi.org/10.1007/bf02285402 Zobrazit plný text záznamu Full text from SpringerLink