Epimeric 24-hydroxyethyl and 24-carboxymethyl steroids were synthesized, their 1H and 13C-NMR spectra recorded and the signals assigned. Based on those assignements information regarding the stereochemistry of the C-24 carbon of the steroids under study was obtained.
CONFIGURATION ASSIGNMENT OF 24R-ISOMERS AND 24S-ISOMERS OF 29-OXYGENATED STEROIDS BY H-1 AND C-13 NMR-SPECTROSCOPY / M. ANASTASIA, P. ALLEVI, P. CIUFFREDA, R. RICCIO. - In: TETRAHEDRON. - ISSN 0040-4020. - 42:17(1986), pp. 4843-4847.
CONFIGURATION ASSIGNMENT OF 24R-ISOMERS AND 24S-ISOMERS OF 29-OXYGENATED STEROIDS BY H-1 AND C-13 NMR-SPECTROSCOPY
M. ANASTASIAPrimo
;P. ALLEVISecondo
;P. CIUFFREDAPenultimo
;
1986
Abstract
Epimeric 24-hydroxyethyl and 24-carboxymethyl steroids were synthesized, their 1H and 13C-NMR spectra recorded and the signals assigned. Based on those assignements information regarding the stereochemistry of the C-24 carbon of the steroids under study was obtained.File in questo prodotto:
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