Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Milena Trmcic"'
Autor:
Zorana Ferjancic, Filip Bihelovic, Bojan Vulovic, Radomir Matovic, Milena Trmcic, Aleksandar Jankovic, Milos Pavlovic, Filip Djurkovic, Radivoje Prodanovic, Aleksandra Djurdjevic Djelmas, Nevena Kalicanin, Mario Zlatovic, Dusan Sladic, Thomas Vallet, Marco Vignuzzi, Radomir N. Saicic
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry, Vol 39, Iss 1 (2024)
AbstractWe developed new iminosugar-based glycosidase inhibitors against SARS-CoV-2. Known drugs (miglustat, migalastat, miglitol, and swainsonine) were chosen as lead compounds to develop three classes of glycosidase inhibitors (α-glucosidase, α-g
Externí odkaz:
https://doaj.org/article/42b63272ecfc453f83c5a84edc1ae71b
Autor:
Zorana Ferjancic, Filip Bihelovic, Bojan Vulovic, Radomir Matovic, Milena Trmcic, Aleksandar Jankovic, Milos Pavlovic, Filip Djurkovic, Radivoje Prodanovic, Aleksandra Djurdjevic Djelmas, Nevena Kalicanin, Mario Zlatovic, Dusan Sladic, Thomas Vallet, Marco Vignuzzi, Radomir N. Saicic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f444cf98048a9518f9004ee82ce9c911
https://doi.org/10.2139/ssrn.4423287
https://doi.org/10.2139/ssrn.4423287
Autor:
N Radomir Saicic, Milena Trmcic
Publikováno v:
Journal of the Serbian Chemical Society
Journal of the Serbian Chemical Society, Vol 86, Iss 12, Pp 1305-1315 (2021)
Journal of the Serbian Chemical Society, Vol 86, Iss 12, Pp 1305-1315 (2021)
An attempt to synthesize the cyclohexane core of antibiotic abyssomicin C is described. The initial, protecting group-free approach (relying on internal protection) failed and had to be modified, in order to allow for efficient deprotection of the ac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9822aad46ad51cb69e9cd17c0ac4e3bc
http://cherry.chem.bg.ac.rs/bitstream/id/29572/bitstream_29572.pdf
http://cherry.chem.bg.ac.rs/bitstream/id/29572/bitstream_29572.pdf
Publikováno v:
Organic Letters
Unsaturated oxyallyl cations with a suitably positioned alkene bond undergo 5-exo-cyclization with the formation of vinylcyclopentane derivatives. Alkyne analogues provide allenes. The reaction proceeds with a moderate to excellent level of stereosel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ba7adfb0f49e0cef5637244acc7145d
https://cherry.chem.bg.ac.rs/handle/123456789/3819
https://cherry.chem.bg.ac.rs/handle/123456789/3819
Autor:
Matija Zlatar, Marko V. Rodić, Radomir N. Saicic, Filip Bihelovic, L. Novkovic, Radomir Matovic, Milena Trmcic
Publikováno v:
RSC Advances
A new Zn(II)-based potential chemotherapeutic agent was synthesized from the ligand 2-quinolinecarboxaldehyde selenosemicarbazone (Hqasesc). Single crystal X-ray diffraction analysis showed that the Zn(II) complex consists of a cation [Zn(Hqasesc)2]2
Autor:
Radomir N. Saicic, Milena Trmcic, Radomir Matovic, Filip Bihelovic, Matija Zlatar, L. Novkovic, Marko V. Rodić
Publikováno v:
ChemInform. 47
Domino reactions of ketones with molecular oxygen in the presence of potassium hydroxide and potassium t-butoxide afford cyclic hydroperoxy acetals (3,5-dihydroxy-1,2-dioxanes). Mixed endoperoxides can also be obtained in a three-component reaction o
Autor:
Biljana Ristic, Gordana Tovilovic, Radomir N. Saicic, Vladimir Trajkovic, Milena Trmcic, Radomir Matovic, Zorana Ferjancic
Publikováno v:
Organic & Biomolecular Chemistry
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry
The design, synthesis and biological evaluation of a novel C, D-spirolactone analogue of paclitaxel is described. This is the first paclitaxel analogue without an oxetane D-ring that shows a significant cytotoxic effect (activity one order of magnitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5576584f442d2583fd688928e327f01d
http://cer.ihtm.bg.ac.rs/handle/123456789/981
http://cer.ihtm.bg.ac.rs/handle/123456789/981
Kinetic studies and predictions on the hydrolysis and aminolysis of esters of 2-S-phosphorylacetates
Autor:
Milena Trmčić, David R. W. Hodgson
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 6, Iss 1, Pp 732-741 (2010)
Background: Heterobifunctional cross-linking agents are useful in both protein science and organic synthesis. Aminolysis of reactive esters in aqueous systems is often used in bioconjugation chemistry, but it must compete against hydrolysis processes
Externí odkaz:
https://doaj.org/article/58be04388cf8437ea65787bb716764af