Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Jovana Muškinja"'
Autor:
D.P. Lydia Renj, R. Racil Jeya Geetha, A. Benifa, M. Amalanathan, M. Sony Michael Mary, Zoran Ratković, Jovana Muškinja, Jayasekar Micheal
Publikováno v:
Chemical Physics Impact, Vol 8, Iss , Pp 100524- (2024)
A systematic spectroscopic investigationof 1-acethyl-2(4-isopropoxy-3-methoxyphenyl) cyclopropanewasperformed by utilizing Density functional theory approaches at B3LYP level usingGaussian 09 W software package. The FT-IR and FT-Raman techniques were
Externí odkaz:
https://doaj.org/article/25acb1fbf3684a0e91535dc242d969a0
Autor:
D.P. Lydia Renj, R. Racil Jeya Geetha, J. Jeni James, M. Amalanathan, M. Sony Michael Mary, Zoran Ratković, Jovana Muškinja
Publikováno v:
Chemical Physics Impact, Vol 8, Iss , Pp 100420- (2024)
To identify promising compounds and to develop a potent non-linear optical material, the molecule 1-acetyl-2-(4-ethoxy-3-methoxyphenyl) cyclopropane (AEMC) was selected. FTIR and FT-Raman spectroscopy techniques were employed to predict the functiona
Externí odkaz:
https://doaj.org/article/6e0e4aa6424b4b46a4f4517353d47423
Autor:
Rastko D. Vukićević, Jovana Muškinja, Goran A. Bogdanović, Sladjana B. Novaković, Zorica Leka
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 12, Pp o1728-o1728 (2013)
In the title compound, C10H12O3, all non-H atoms are approximately coplanar, with an r.m.s. deviation of 0.046 Å. In the crystal, very weak C—H...O interactions link the molecules into sheets parallel to (101).
Externí odkaz:
https://doaj.org/article/dc7245900b9a4f8fafc472afb741a7a7
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 11, Pp o1625-o1625 (2013)
In the title compound, C11H14OS, all non-H atoms are essentially coplanar, with a mean deviation of 0.023 Å. In the crystal, centrosymmetrically related molecules are weakly connected into dimers by pairs of C—H...O interactions. The dimers are fu
Externí odkaz:
https://doaj.org/article/7cfe692d4a714b02951d0801c3ede031
Autor:
Marija Anđelković, Ivana Nikolić, Jovan Luković, Marina Mitrović, Ivanka Zelen, Jovana Muškinja, Zoran Ratković, Suzana Popović, Sanja Stanković, Marijanа Stanojević Pirković
Publikováno v:
Serbian Journal of Experimental and Clinical Research.
Chalcones represent a type of flavonoids which are located at vegetative and reproductive organs of plants and they can be metabolic progenitor molecules for several flavonoids and isoflavonoids. Many studies indicated that molecular structure of cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffa474a7a70860a33f4ae9ade2022a24
https://doi.org/10.2478/sjecr-2021-0065
https://doi.org/10.2478/sjecr-2021-0065
Autor:
Nenad Joksimović, Zoran Ratković, Emilija Milović, Jovana Muškinja, Milan Vraneš, Srđan Stefanović, Nenad Janković, Jelena Petronijević
Publikováno v:
Environmental Chemistry Letters. 19:729-736
© 2020, Springer Nature Switzerland AG. Reactions in water as a safe and cheap solvent is a major goal of green chemistry. Actual synthesis of pyrido-dipyrimidine scaffold, named DNA-base hybrids, involves catalysis in hazardous solvents. Here we sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6def836c232ba7607467adb7cfb58e32
https://doi.org/10.1007/s10311-020-01076-9
https://doi.org/10.1007/s10311-020-01076-9
Autor:
Marina Mitrovic, Marija Sorak, Zoran Ratković, Jovan Lukovic, Marija Anđelković, Jovana Muškinja, Marijana Stanojevic-Pirkovic, Ivanka Zelen, Zoran Milosavljevic, Ivana Nikolic, Suzana Popovic
Publikováno v:
Acta Poloniae Pharmaceutica - Drug Research. 77:57-67
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::440bf416264f7a938729292f6b713193
https://doi.org/10.32383/appdr/112786
https://doi.org/10.32383/appdr/112786
Autor:
Milan Zaric, Danijela Todorović, Adrijana Burmudžija, Suzana Popovic, Zoran Ratković, Jovana Muškinja, Dejan Baskic
Publikováno v:
Medicinal Chemistry Research. 28:279-291
Three series of sulfonyl esters were synthesized in reactions of sulfonyl chlorides with three different phenolic chalcone analogues (dehydrozingerone (4-(4-hydroxy-3-methoxyphenyl)-3-buten-2-one), (E)-1-(4-hydroxy-3-methoxyphenyl)pent-1-en-3-one, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::192e954b50212c0493d80297f8ed5683
https://doi.org/10.1007/s00044-018-02283-4
https://doi.org/10.1007/s00044-018-02283-4
Publikováno v:
Proceedings of 6th International Electronic Conference on Medicinal Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09d14fc5d8bce252b13e776441fdb54e
https://doi.org/10.3390/ecmc2020-07422
https://doi.org/10.3390/ecmc2020-07422
Autor:
Zoran Ratković, Jovan Lukovic, Tanja Zecevic-Lukovic, Marija Anđelković, Jovana Muškinja, Ivana Nikolic, Marina Mitrovic, Marina Živić
Publikováno v:
Proceedings of 6th International Electronic Conference on Medicinal Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42dc95db5142941459154270caceb407
https://doi.org/10.3390/ecmc2020-07429
https://doi.org/10.3390/ecmc2020-07429