Zobrazeno 1 - 10
of 112
pro vyhledávání: '"Radomir N Saicic"'
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:
Ksenija D. Glusac, Radomir N. Saicic
Publikováno v:
Nature Chemistry. 15:439-442
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:
Journal of the Serbian Chemical Society, Vol 72, Iss 12, Pp 1173-1179 (2007)
Homoallylic radicals, generated from the corresponding xanthates, react with terminal alkynes to give cyclopentene derivatives in moderate yields.
Externí odkaz:
https://doaj.org/article/94115dcf3e0a40a2bd2bf20af3cfc54c
Publikováno v:
Journal of the Serbian Chemical Society, Vol 71, Iss 7, Pp 713-720 (2006)
The new compounds 1-aryl-3-{1-phenyl-3-[p-(methylthio)phenyl]pyrazol-4-yl}-2-propen-1-ones 2a–l were prepared by the condensation of 1-phenyl-3-[p-(methylthio)phenyl]-4-formylpyrazole 1 with different aryl ketones. Compounds 2a–l in reaction with
Externí odkaz:
https://doaj.org/article/8a2cd3c9b52e44c0b23b8a983ca3b512
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
Publikováno v:
Journal of the Serbian Chemical Society, Vol 69, Iss 11, Pp 981-990 (2004)
A method for the stereoselective homologation of a-amino acids into syn-a-hydroxy-b-amino acids is described, based on the conversion of stereoisomeric cyanohydrins into trans-oxazolines. The synthetic potential of the method is illustrated in the en
Externí odkaz:
https://doaj.org/article/09f43e81cc8b411da5311ec09a6eb159
Publikováno v:
Journal of the Serbian Chemical Society, Vol 69, Iss 10, Pp 737-747 (2004)
A stereoselective free radical introduction of a phenylthio group onto a nonactivated methyl group in the d-position, adjacent to a prochiral carbon atom, was achieved by photolysis of (-)-menthyl benzenesulfenate in the presence of hexabutylditin an
Externí odkaz:
https://doaj.org/article/50797fe2c9aa477083a0ba7967eeec28
Publikováno v:
Journal of the Serbian Chemical Society, Vol 67, Iss 4, Pp 221-227 (2002)
In this model study an alternative synthetic approach to the C1C7 fragment of epothilones was investigated. Starting from 4,4-dimethylcyclopentenone, a 7 step reaction sequence afforded the key intermediate 7 in 27 % overall yield. Surprisingly, the
Externí odkaz:
https://doaj.org/article/ef8594e5fb93452ca102bfe071cd0847