Total synthesis and properties of prostaglandins 30. Modification of (1S,5R)-2-oxabicyclo[3.3.0]-6-octen-3-one at the ?-carbon atom

Autor:	M. P. Gavars, T. V. Mazur, Ya. F. Freimanis, I. V. Turovskii, K. I. Dikovskaya
Rok vydání:	1991
Předmět:	chemistry.chemical_compound Carbon atom Bicyclic molecule chemistry Stereochemistry Organic Chemistry Total synthesis Prostaglandin Carbonyl group
Zdroj:	Chemistry of Heterocyclic Compounds. 27:1300-1308
ISSN:	1573-8353 0009-3122
DOI:	10.1007/bf00515573
Popis:	Derivatives of α-alkyl-, α-alkylidene-, and α-hydroxymethylene-2-oxabicyclo[3.3.0]-6-octen-3-one were obtained. The possibility of functional substitution of the bicyclic γ-lactones at the α position to the carbonyl group was thereby demonstrated.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::a3ae678fddc65191b11d6128f9e96ee6 https://doi.org/10.1007/bf00515573 Zobrazit plný text záznamu Full text from SpringerLink