Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Petrović, Julijana A."'
Autor:
Petrović Julijana A., Sakač Marija N., Penov-Gaši Katarina M., Pejanović Vjera M., Jovanović-Šanta Suzana S.
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://doaj.org/article/95551fa6bdb64c03aad082d01d0bd413
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://doaj.org/article/83e1aaee57d04af398ed2eac8d66efa3
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(
Externí odkaz:
https://doaj.org/article/f8bc31b4746544848e8d358cfb954153
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
Externí odkaz:
https://doaj.org/article/e2ed756bd8ef48ae9afc18e01c1aa5bb
Publikováno v:
Book of Proceedings / 1st International Conference on Chemo and BioInformatics, ICCBIKG 2021; October 26-27, 2021; Kragujevac, Serbia
About 75% of breast cancers express estrogen receptors (ERs), which is a good base for an efficient endocrine therapy. This gives the opportunity for the treatment of patients with antiestrogens, compounds that bind to the ERs and thus compete to est
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4175::86c50cc5b8196980e7e724e3d434fae6
https://vinar.vin.bg.ac.rs/handle/123456789/10882
https://vinar.vin.bg.ac.rs/handle/123456789/10882
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Jovanović-Šanta, Suzana1 santas@ih.ns.ac.yu, Petrović, Julijana1, Andrić, Silvana2, Kovačević, Radmila2, Durendić, Evgenija1, Sakač, Marija1, Lazar, Dušan3, Stanković, Slobodanka3
Publikováno v:
Bioorganic Chemistry. Dec2003, Vol. 31 Issue 6, p475. 10p.
Publikováno v:
Chromatographia; January 1984, Vol. 18 Issue: 1 p37-40, 4p
Autor:
Penov-Gaši, Katarina, Miljković, Dušan, Medić-Mijačević, Ljubica, Durendić, Evgenija, Petrović, Julijana, Pejanović, Vjera, Stanković, Slobodanka, Lazar, Dušan
Publikováno v:
Tetrahedron Letters; January 1998, Vol. 39 Issue: 52 p9759-9760, 2p