Complete H-1 and C-13 spectral assignments of 17beta- and 17alpha-hydroxy epimers of three biologically active sterols (boldenone, 3-methoxyestradiol and 3-methoxydihydroequilenin) were achieved making use of one- and two-dimensional NMR techniques (1D-HOHA, DEPT, COSY, NOESY, TOCSY, HSQC and COLOC).
Complete H-1 and C-13 NMR spectral assignment of 17-hydroxy epimeric sterols with planar A or A and B rings / P. Ciuffreda, S. Casati, A. Manzocchi. - In: MAGNETIC RESONANCE IN CHEMISTRY. - ISSN 0749-1581. - 42:3(2004), pp. 360-363.
Complete H-1 and C-13 NMR spectral assignment of 17-hydroxy epimeric sterols with planar A or A and B rings
P. CiuffredaPrimo
;S. CasatiSecondo
;A. ManzocchiUltimo
2004
Abstract
Complete H-1 and C-13 spectral assignments of 17beta- and 17alpha-hydroxy epimers of three biologically active sterols (boldenone, 3-methoxyestradiol and 3-methoxydihydroequilenin) were achieved making use of one- and two-dimensional NMR techniques (1D-HOHA, DEPT, COSY, NOESY, TOCSY, HSQC and COLOC).
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