Zobrazeno 1 - 10
of 137
pro vyhledávání: '"Mirjana Popsavin"'
Autor:
Sladjana Stanisavljevic, Bojana Sreco-Zelenovic, Mirjana Popsavin, Marko Rodic, Velimir Popsavin, Vesna Kojic
Publikováno v:
Journal of the Serbian Chemical Society. 88:113-121
Four novel conformationally restricted (?)-muricatacin analogues, bearing a methoxy group at the C-5 position and with an alkoxymethyl group ?s the C-7 side chain, have been synthesised and their in vitro antiproliferative activity was evaluated agai
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1bfa786eea046bfd58258fe76c54e0e8
https://doi.org/10.2298/jsc220613069s
https://doi.org/10.2298/jsc220613069s
Autor:
Ljubica Grbović, Bojana Radovan Vasiljević, Ksenija Pavlović, Timea Hajnal-Jafari, Simonida Đurić, Mirjana Popsavin, Slavko Kevrešan
Publikováno v:
Macedonian Journal of Chemistry and Chemical Engineering, Vol 37, Iss 1, Pp 13-20 (2018)
Within the field of green chemistry, a noticeable results were obtained in the solvent-free synthesis of amide derivatives of naphthenic acids under microwave irradiation. Naphthenic acid amides, anilides, and morpholides were synthesized directly fr
Externí odkaz:
https://doaj.org/article/0dbcf19cd0294398abfbf27d269fb44e
Autor:
Jovana Francuz, Sanja Djokić, Mirjana Popsavin, Marko V. Rodić, Vesna Kojić, Biljana Krüger, Velimir Popsavin
Publikováno v:
Synlett.
A new synthetic approach to protulactone A and several of its structural analogues, starting from d-galactose, has been developed. In a preliminary bioassay, all the compounds showed potent cytotoxicities. A structure–activity relationship analysis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::83020a6fe26bd19038e995f8b3566c68
https://doi.org/10.1055/s-0042-1751400
https://doi.org/10.1055/s-0042-1751400
Autor:
Sanja Djokić, Jovana Francuz, Mirjana Popsavin, Marko V. Rodić, Vesna Kojić, Milena Stevanović, Velimir Popsavin
Publikováno v:
Bioorganic chemistry. 127
Synthesis of protulactone A (PLA, 1) and twelve of its analogues have been achieved starting from D-galactose. PLA was isolated in the crystalline state, and its crystal structure was determined utilizing X-ray crystallography, which confirmed the as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b431c98c1489a03b00126a50f9f689f4
https://pubmed.ncbi.nlm.nih.gov/35772366
https://pubmed.ncbi.nlm.nih.gov/35772366
Autor:
Mirjana Popsavin, Sanja Grabež, Jovana Francuz, Vesna Kojić, Bojana Srećo Zelenović, Velimir Popsavin
Publikováno v:
Journal of the Serbian Chemical Society, Vol 85, Iss 12, Pp 1539-1551 (2020)
Several (+)-goniofufurone analogues with simplified structures were designed, synthesized and evaluated for their in vitro antitumour activity, against a panel of human tumour cell lines. Dephenylated compounds 2 and 3 demonstrated remarkable antitum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1740babfe368b1ba85c307f69a1f6c72
https://doi.org/10.2298/jsc200730056s
https://doi.org/10.2298/jsc200730056s
Autor:
Miloš Svirčev, Mirjana Popsavin, Aleksandar Pavić, Branka Vasiljević, Marko V. Rodić, Sanja Djokić, Jelena Kesić, Bojana Srećo Zelenović, Velimir Popsavin, Vesna Kojić
Publikováno v:
Bioorganic Chemistry. 121
The synthesis of several new goniofufurone bioisosteres was achieved in which the phenyl residue was replaced by a thiazole ring. The key steps of the synthesis included the initial condensation of cyanohydrin benzoates with cysteine ethyl ester hydr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f312d8bce01f6edd423a81e84fed6df
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85124994961&origin=inward
https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85124994961&origin=inward
Autor:
Sándor Farkas, Goran Benedekovic, Sladjana Stanisavljevic, Bojana Sreco-Zelenovic, Mirjana Popsavin, Velimir Popsavin, Dimitar Jakimov
Publikováno v:
Journal of the Serbian Chemical Society. :18-18
(5R)-Cleistenolide and a few related analogues have been synthesized starting from d-glucose. The key steps of the synthesis included a Z-selective Wittig olefination and an intramolecular Mitsunobu reaction with an inversion of configuration at the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a705af4c7bed0111b30df34e249079ac
https://doi.org/10.2298/jsc230126018f
https://doi.org/10.2298/jsc230126018f
Autor:
Vesna Kojic, Milos Svircev, Sanja Djokic, Ivana Kovacevic, Marko Rodic, Bojana Sreco-Zelenovic, Velimir Popsavin, Mirjana Popsavin
Publikováno v:
Journal of the Serbian Chemical Society. :2-2
New thiazole hybrids were synthesized and evaluated for their in vitro cytotoxicity against a panel of human malignant cell lines. The key steps in the synthesis of hybrids 3?7 involved the initial condensation of appropriate aldo-nonitriles with cys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe3844f9430b0b1c0a96896dede36ef6
https://doi.org/10.2298/jsc221130002k
https://doi.org/10.2298/jsc221130002k
Autor:
VESNA NIKOLIC, LJUBISA NIKOLIC, MIHAJLO STANKOVIC, AGNES KAPOR, MIRJANA POPSAVIN, DRAGAN CVETKOVIC
Publikováno v:
Journal of the Serbian Chemical Society, Vol 72, Iss 8-9, Pp 737-746 (2007)
The molecular inclusion complex of atenolol with 2-hydroxypropyl-b-cyclodextrin was synthesized using the coprecipitation method. The complex obtained was characterized by FT-IR, 1H‑NMR, 13C-NMR spectroscopy, as well as by DSC and X-ray diffracti
Externí odkaz:
https://doaj.org/article/10bc46f3e70a4c8d8a11ce8e9ed93911
Autor:
Miloš Svirčev, Mirjana Popsavin, Aleksandar Pavić, Branka Vasiljević, Marko V. Rodić, Sanja Djokić, Jelena Kesić, Bojana Srećo Zelenović, Velimir Popsavin, Vesna Kojić
Publikováno v:
Bioorganic Chemistry. 127:105984
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66ee74ecf9e800f2883a17611a945fba
https://doi.org/10.1016/j.bioorg.2022.105984
https://doi.org/10.1016/j.bioorg.2022.105984