Zobrazeno 1 - 10
of 20
pro vyhledávání: '"A Julijana Petrovic"'
Autor:
Suzana Jovanović-Šanta, Mihály Szécsi, Olivera R. Klisurić, Radmila Kovacevic, Edward T. Petri, Julijana Petrovic
Since many estrogen derivatives exhibit anti-hormone or enzyme inhibition potential, a large number of steroidal derivatives have been synthesised from appropriate precursors, in order to obtain potential therapeutics for the treatment of hormone-dep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06c6c9b1847dddaae23afda5f2df81cb
http://publicatio.bibl.u-szeged.hu/5919/
http://publicatio.bibl.u-szeged.hu/5919/
Autor:
N Marija Sakac, Suzana Jovanović-Šanta, M Katarina Penov-Gasi, A Julijana Petrovic, M Vjera Pejanovic
Publikováno v:
Acta Periodica Technologica, Vol 2004, Iss 35, Pp 225-230 (2004)
In this paper two synthetic routes for obtaining D-homo-D-aza estratriene derivatives were described. Namely, starting from 3-methoxyestra-1,3,5(10)-trien-16-oximino-17-one (1) 3-methoxy-17-aza-D-homoestra-1,3,5(10)-triene (5) was synthesized in two
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::033589de9d116459ebc4950fe0bcd652
https://doi.org/10.2298/apt0435225p
https://doi.org/10.2298/apt0435225p
Autor:
Suzana Jovanović-Šanta, Dušan Lazar, Slobodanka Stanković, Marija N. Sakač, Evgenija A. Đurendić, Julijana Petrovic, Silvana A. Andric, Radmila Kovacevic
Publikováno v:
Bioorganic Chemistry. 31:475-484
The starting compound for synthesis of new 16,17-seco-estratriene derivatives was 3-benzyloxy-17-hydroxy-16,17-secoestra-1,3,5(10)-triene-16-nitrile (1b), obtained from estrone in several synthetic steps. 17-Tosyl, -chloro-, bromo-, and -iodo- deriva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fa306d062bc1ee55926b5b07a7893b6e
https://doi.org/10.1016/s0045-2068(03)00101-9
https://doi.org/10.1016/s0045-2068(03)00101-9
Publikováno v:
Zbornik Matice Srpske za Prirodne Nauke, Vol 2002, Iss 103, Pp 5-9 (2002)
Under the conditions of Beckmann fragmentation reaction 3-benzyloxy-17(-hydroxyestra-1, 3, 5, (10)-triene-16-one oxime (2) gave the D-seco derivative 3. Sodium borohydride reduction of this compound afforded 3-benzyloxy-17-hydroxy-16, 17-secoestra-1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ec68f73bfa79ec02b9306b35351f9f4
https://doi.org/10.2298/zmspn0201005j
https://doi.org/10.2298/zmspn0201005j
Publikováno v:
Journal of the Serbian Chemical Society, Vol 65, Iss 11, Pp 811-818 (2000)
The effect of C-18 silica gel surface coverage on the retention behaviour of some estrone derivatives in reversed phase high performance liquid chromatography has been studied. Two commercial columns with different C-18 coverage, Spherisorb ODS-1(8 %
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d2c4e75f74a81e13956597cbf2f85c0
https://doi.org/10.2298/jsc0011811a
https://doi.org/10.2298/jsc0011811a
Publikováno v:
Journal of the Serbian Chemical Society, Vol 64, Iss 5-6, Pp 391-394 (1999)
Starting from 3-benzyloxy-17-hydroxy-16,17-secoestra-1,3,5(10)-triene-16-nitrile (1b), 17-tosylate 2b and also 17-chloro-, 17-bromo- and 17-iodo-derivatives 4b, 5b, and 6b, were obtained. The fluoro-derivative 3b was obtained from2b in the reaction w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c2bbe53a96fcaac2c655609f50f0ded
http://www.doiserbia.nb.rs/img/doi/0352-5139/1999/0352-51399906391J.pdf
http://www.doiserbia.nb.rs/img/doi/0352-5139/1999/0352-51399906391J.pdf
Publikováno v:
Chromatographia. 43:551-556
The chromatographic behaviour of 30 estradiol and estrone derivatives has been studied on diol, amino- and cyanopropyl silica gel stationary phases with non-aqueous mobile phases. The slopes of linear relationships between the logarithm of the retent
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0227bc69f2149330ce62412183cdeacb
https://doi.org/10.1007/bf02293009
https://doi.org/10.1007/bf02293009
Autor:
Julijana Petrovic, Vjera Pejanovic, A. Stefanović, D. Miljkovic, Slobodanka Stanković, M. Bruvo
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::244c9a32aa42347148861115890257f6
https://doi.org/10.1002/chin.199518218
https://doi.org/10.1002/chin.199518218
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::36ab67f54e38a999cf4a2764d0f1632c
https://doi.org/10.1002/chin.199613220
https://doi.org/10.1002/chin.199613220
Autor:
Ljubica Medić-Mijačević, Dušan Miljković, Slobodanka Stanković, Dušan Lazar, Vjera Pejanovic, Julijana Petrovic, Evgenija Durendic, Katarina Penov-Gaši
Publikováno v:
ChemInform. 30
By a novel “one pot” fragmentation-cyclization reaction 17β-hydroxy-17α-substituted-16-oximino derivatives in the androstane and estrane series were converted to a new type of D-homo derivative.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::242ea4f5a4db8d313184aa0065909233
https://doi.org/10.1002/chin.199913224
https://doi.org/10.1002/chin.199913224