Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Rabdan M. Tikhov"'
Autor:
Ekaterina A Glubokova, Irina A. Leneva, Nikolai Yu. Kuznetsov, Rabdan M. Tikhov, Nadezda P. Kartashova, Irina N. Falynskova
Publikováno v:
Acta Naturae
The World Health Organization (WHO) recommends antivirals as an additional line of defense against influenza. One of such drugs is rimantadine. However, most of the circulating strains of influenza A viruses are resistant to this drug. Thus, a search
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac169da99d6394a729c67a9af813802e
https://doi.org/10.32607/actanaturae.11020
https://doi.org/10.32607/actanaturae.11020
Publikováno v:
Organic & Biomolecular Chemistry. 18:2793-2812
The current review summarizes the latest achievements in the synthesis of piperidine-2,4-dione-type azaheterocycles. Two main groups traditional (carbonyl compound transformations) and novel (anionic enolate rearrangements) of complementary methods f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89123effa84526e3b6ef1575801cb55d
https://doi.org/10.1039/d0ob00287a
https://doi.org/10.1039/d0ob00287a
Autor:
E.S. Kirillova, Ivan A. Godovikov, Nikolai Yu. Kuznetsov, Yuri N. Bubnov, Elena Burtseva, Konstantin A. Lyssenko, Michael G. Medvedev, Rabdan M. Tikhov
Publikováno v:
Organic & Biomolecular Chemistry. 15:3152-3157
A series of (R)- and (S)-isomers of new adamantane-substituted heterocycles (1,3-oxazinan-2-one, piperidine-2,4-dione, piperidine-2-one and piperidine) with potent activity against rimantadine-resistant strains of influenza A virus were synthesized t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a5df7e2022e7793d2289f611122ddea
https://doi.org/10.1039/c7ob00331e
https://doi.org/10.1039/c7ob00331e
Autor:
Yuri N. Bubnov, Nikolai Yu. Kuznetsov, Konstantin A. Lyssenko, Rabdan M. Tikhov, Tatyana V. Strelkova
Publikováno v:
Tetrahedron Letters. 57:4525-4528
A new and efficient method for the synthesis of 6-amino-2,3-dihydro-4-pyridinethiones from N -(3-butenyl)thioureas, without the use of conventional thiophosphorus reagents has been reported. Thioureas are initially transformed into iodocyclothiocarba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30d82b84efd8094c8f735a1863abb0dc
https://doi.org/10.1016/j.tetlet.2016.08.010
https://doi.org/10.1016/j.tetlet.2016.08.010
Publikováno v:
Organicbiomolecular chemistry. 16(39)
Dimethylamine adducts of triallyl-, triprenyl- and trans-cinnamyl(dipropyl)borane are effective reagents for mild homoallylation of primary amines with aqueous formaldehyde in MeOH without an inert atmosphere. A new concept is proposed for the explan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb212adf48134fadf54dd8cc9a79bd99
https://pubmed.ncbi.nlm.nih.gov/30250957
https://pubmed.ncbi.nlm.nih.gov/30250957
Publikováno v:
Organic letters. 20(12)
Triallylborane–amines adducts are effective stoichiometric allylating agents in the aminoallylation reaction of carbonyl compounds in methanol. Moreover, copper-catalyzed diastereoselective allylation of Ellman’s imine was achieved with triallylb
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d36dbf2e52d061dc47a9a96990184cb3
https://pubmed.ncbi.nlm.nih.gov/29873233
https://pubmed.ncbi.nlm.nih.gov/29873233
Publikováno v:
Organicbiomolecular chemistry. 14(18)
Three-step synthesis of 6-amino-2,3-dihydro-4-pyridinones from homoallylamines involving NBS-mediated cyclization of N-(3-butenyl)ureas to 6-(bromomethyl)-2-iminourethanes, dehydrohalogenation and a novel rearrangement as a key step has been develope
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f501b14c118c82b234cd5f264a12cfce
https://pubmed.ncbi.nlm.nih.gov/27080757
https://pubmed.ncbi.nlm.nih.gov/27080757