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. ANASTASIA
Primo
;
P. ALLEVI
Secondo
;
P. CIUFFREDA
Penultimo
;
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.
Settore BIO/12 - Biochimica Clinica e Biologia Molecolare Clinica
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/182393
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