Literature DB >> 14971022

Complete 1H and 13C NMR spectral assignment of 17-hydroxy epimeric sterols with planar A or A and B rings.

P Ciuffreda1, S Casati, A Manzocchi.   

Abstract

Complete 1H and 13C 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-HOHAHA, DEPT, COSY, NOESY, TOCSY, HSQC and COLOC). Copyright 2004 John Wiley & Sons, Ltd.

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Year:  2004        PMID: 14971022     DOI: 10.1002/mrc.1342

Source DB:  PubMed          Journal:  Magn Reson Chem        ISSN: 0749-1581            Impact factor:   2.447


  2 in total

1.  1H and 13C NMR characterization and stereochemical assignments of bile acids in aqueous media.

Authors:  Omkar B Ijare; B S Somashekar; Y Jadegoud; G A Nagana Gowda
Journal:  Lipids       Date:  2005-10       Impact factor: 1.880

2.  Simple Synthesis of 17-β-O-hemisuccinate of Stanozolol for Immunoanalytical Methods.

Authors:  Silvana Casati; Roberta Ottria; Pierangela Ciuffreda
Journal:  Molecules       Date:  2020-04-26       Impact factor: 4.411

  2 in total

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