Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Filip Bihelovic"'
Autor:
RATKO JANKOV, FILIP BIHELOVIĆ, DEJAN BEZBRADICA, DUŠAN VELIČKOVIĆ, ALEKSANDRA DIMITRIJEVIĆ, NENAD MILOSAVIĆ
Publikováno v:
Journal of the Serbian Chemical Society, Vol 76, Iss 8, Pp 1081-1092 (2011)
The production of lipase from Pseudozyma aphidis (DSM 70725) was determined in six different media. The highest lipase production was observed in a medium with glucose as the sole carbon source, and yeast extract and sodium nitrate as the nitrogen
Externí odkaz:
https://doaj.org/article/89cb650bc98e4d82980a298b790ffbbe
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
Publikováno v:
Natural Product Communications
Natural Product CommunicationsNatural Product Communications
Natural Product CommunicationsNatural Product Communications
A tactical combination of either ( S)- or ( R)-proline catalyzed aldol reaction followed by intramolecular reductive amination enabled the synthesis of a chiral pyrrolidine derivative with 3 contiguous stereocenters in only 2 synthetic steps, startin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e2dda569298ef3896f92ac99818c8e9
http://cherry.chem.bg.ac.rs/bitstream/id/30082/Total_synthesis_of.pdf
http://cherry.chem.bg.ac.rs/bitstream/id/30082/Total_synthesis_of.pdf
Publikováno v:
Israel Journal of Chemistry
The advent of gold catalysis has transformed hydroxyalkoxylation of alkynes - once a rudimentary, mercury(II)-, or silver(I)-catalyzed process limited to structurally simple substrates - into a sophisticated method that has found application in synth
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 25(17)
A chiral-pool-based synthesis of the platensimycin core was achieved using (S)-lactic acid as an inexpensive starting material. The cyclohexenone ring was closed in a Mukaiyama-Michael domino sequence, while the quaternary stereocenter was created by
Publikováno v:
Chemistry-A European Journal
A chiral-pool-based synthesis of the platensimycin core was achieved using (S)-lactic acid as an inexpensive starting material. The cyclohexenone ring was closed in a Mukaiyama–Michael domino sequence, while the quaternary stereocenter was created
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b42271f32b628ae0add1a92cccb2128
https://cherry.chem.bg.ac.rs/handle/123456789/2874
https://cherry.chem.bg.ac.rs/handle/123456789/2874
Publikováno v:
Journal of the Serbian Chemical Society
Journal of the Serbian Chemical Society, Vol 84, Iss 9, Pp 935-941 (2019)
Journal of the Serbian Chemical Society, Vol 84, Iss 9, Pp 935-941 (2019)
Two new analogues of alstoscholarisine A, containing a phenyl or butyl substituent at the C-19 position, have been prepared in racemic form from the known skatole derivative. The syntheses of these compounds were accomplished in 13 steps, with a late
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d51fc640df3c3bc3840df6e6d396fef
https://cherry.chem.bg.ac.rs/handle/123456789/3660
https://cherry.chem.bg.ac.rs/handle/123456789/3660
Autor:
Filip Bihelovic, Zorana Ferjancic
Publikováno v:
Angewandte Chemie (International Edition)
The first total synthesis of the neuroactive indole alkaloid (+/-)-alstoscholarisine A is reported. The key step of the concise synthesis is an efficient domino sequence that was used to assemble the 2,8-diazabicyclo[3.3.1]nonane core through the for
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