Chemical behavior of 3,17β-dipropionoxy-9α-hydroxyestra-1,3,5(10)-trien-6-one

Journal of the Serbian Chemical Society

Volumn 63, Issue 1, 1998, Pages 21-24

  Sakač, Marija N ^a   Miljković, Dus̀an A ^a   Penov Gaši, Katarina M ^a   Petrović, Julijana A ^a  

^a UNIVERSITY OF NOVI SAD   (Serbia)

Author keywords

Estradiol derivatives; Oxidation of estradiol dipropionate

Indexed keywords

EID: 0007567392     PISSN: 03525139     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. J. Bowler, T. J. Lilley, J. D. Pittam, A. E. Wakeling, Steroids 54 (1989) 71
2. X. Qian, Y. Y. Abul-Hajj, Steroids 55 (1990) 238
3. V. Pejanović, Ph. D. Thesis, University of Novi Sad, 1991
4. V. M. Pejanović, J. A. Petrović, D. D. Djoković, D. A. Miljković, Review of Research, Faculty of Sciences - University of Novi Sad, 21 (1991) 31
5. Gy. Agray, A. Kálman, B. Ribár, M. Sakač, D. Miljković, Zeitschrift für Kristallographie 210 (1995) 785
6. 13C-NMR spectra were recorded with a Brucker AC 250E instrument, with tetramethylsilane as the internal standard. The chemical shifts are given in ppm (δ-scale). The mass spectra were measured using a Finnigan-MAT 8230 (the first number denotes the m/z value, and the ion abundances are given in parentheses). The melting points were determined with a Büchi SMP-20 apparatus and are uncorrected.