Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Zorana Ferjancic"'
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
Publikováno v:
Journal of the Serbian Chemical Society, Vol 71, Iss 7, Pp 705-711 (2006)
The reaction of a-(20)-epoxy-5-O-mesyltriacetyltaxicine I (2) with BF3·Et2O/Bu4NBr can give rise to 4 different products. Each of these products can be obtained selectively, under the appropriate reaction conditions.
Externí odkaz:
https://doaj.org/article/f57b7e76c3e94594a68efed2b89d1a9e
Autor:
Radomir N. Saičić, Zorana Ferjancic
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis. :1-19
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:
European Journal of Organic Chemistry. 2017:6146-6153
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