Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Dzhul'etta V. Avetisyan"'
Publikováno v:
ChemistrySelect. 5:7835-7839
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::769dc1f471b4144652e30dc11ef8d317
https://doi.org/10.1002/slct.201904255
https://doi.org/10.1002/slct.201904255
Autor:
Lyudmila V. Afanas’eva, Irena S. Akhrem, Dzhul’etta V. Avetisyan, Nikolai D. Kagramanov, Oleg I. Artyushin
Publikováno v:
Mendeleev Communications. 30:238-240
A simple and efficient one-pot synthesis of benzophenone Schiff bases from benzene, CCl4 and aromatic amines was developed based on the the reaction of benzene with CCl4·AlCl3 complex. This method affords Ph2CCl2 as well as the products of its subse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::121e578f05a242d6ad5542c446514267
https://doi.org/10.1016/j.mencom.2020.03.037
https://doi.org/10.1016/j.mencom.2020.03.037
Autor:
Andrey L. Sigan, Lyudmila V. Afanas’eva, Nikolai D. Kagramanov, Irena S. Akhrem, Dzhul’etta V. Avetisyan, Oleg I. Artyushin
Publikováno v:
Tetrahedron Letters. 58:4014-4019
The one-pot, regioselective synthesis of branched diacid derivatives – diesters, dithioesters, diamides [YC(O)O(CH2)mC(Me)2OC(O)Y] and diketones of aromatic and heteroaromatic series, [ArCO(CH2)mC(Me)2C(O)Ar,) from available linear acyl halides, Cn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d46d55f49ddbcadb9aaa313d71153ad
https://doi.org/10.1016/j.tetlet.2017.09.019
https://doi.org/10.1016/j.tetlet.2017.09.019
Autor:
Irena S. Akhrem, Dzhul’etta V. Avetisyan, Lyudmila V. Afanas’eva, Oleg I. Artyushin, Nikolai D. Kagramanov
Publikováno v:
Tetrahedron Letters. 56:562-566
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bdda1da2233537ed6b490de3a3d83c1a
https://doi.org/10.1016/j.tetlet.2014.11.115
https://doi.org/10.1016/j.tetlet.2014.11.115
Autor:
Irena S. Akhrem, Dzhul’etta V. Avetisyan, Oleg I. Artyushin, A. A. Tyutyunov, Nikolai D. Kagramanov, Lyudmila V. Afanas’eva
Publikováno v:
Mendeleev Communications. 28:651-652
One-pot functionalization of sp3 C–H bond in 1,1,1-trifluoro-2-(trifluoromethyl)decan-2-ol with CO and nucleophiles under the action of superelectrophilic complex CBr4·2 AlBr3 affords products of neo-structure and remote functionalities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f8d93e67159ecc14d8548dfd7041b83
https://doi.org/10.1016/j.mencom.2018.11.030
https://doi.org/10.1016/j.mencom.2018.11.030
Autor:
Irena S. Akhrem, Dzhul’etta V. Avetisyan, Irina M. Churilova, Lyudmila V. Afanas’eva, Oleg I. Artyushin, Nikolai D. Kagramanov
Publikováno v:
Tetrahedron Letters. 54:6037-6040
The one-pot, regioselective, remote functionalization of amides of octanoic acid [R 2 NCOC 7 H 15 , NR 2 = NH 2 , NEt 2 , NC 4 H 8 O, (morpholinyl)] via Csp 3 –H bond cleavage with CO and various nucleophiles (EtOH, i PrOH, CF 3 CH 2 OH, H(CF 2 ) 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb04bea9f2ac71206ef18f35d7253398
https://doi.org/10.1016/j.tetlet.2013.08.087
https://doi.org/10.1016/j.tetlet.2013.08.087
Publikováno v:
Tetrahedron Letters. 53:3493-3496
A new approach to a simple one-pot functionalization of adamantane and 1,3-dimethyladamantane with CO and various nucleophiles in the presence of the superelectrophilic complex, CBr4·2AlBr3 provides access to important 1,3-dicarbonyl adamantanes wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d19852c6d6c7f7fe858df2d8e12b7514
https://doi.org/10.1016/j.tetlet.2012.04.125
https://doi.org/10.1016/j.tetlet.2012.04.125
Autor:
Alexander Orlinkov, Nikolai D. Kagramanov, Dzhul’etta V. Avetisyan, Irena S. Akhrem, Pavel V. Petrovskii, Lyudmila V. Afanas’eva
Publikováno v:
Tetrahedron Letters. 51:907-911
A novel ‘alkane-like’ methodology for the direct and very simple one-pot functionalization of amides and an ester of 1-adamantanecarboxylic acid provides access to new and synthetically challenging 1,3-dicarbonyl-containing adamantanoid compounds
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fdd971f7922ae152faf79b90ce84ff6
https://doi.org/10.1016/j.tetlet.2009.12.022
https://doi.org/10.1016/j.tetlet.2009.12.022
Superelectrophilic sp3 C–H carbonylation of n-octyl acetate as a way to new bifunctional neo-octanes
Autor:
Nikolai D. Kagramanov, Alexander Orlinkov, Lyudmila V. Afanas’eva, Irena S. Akhrem, Dzhul’etta V. Avetisyan, Pavel V. Petrovskii
Publikováno v:
Mendeleev Communications. 21:323-325
Carbonylation of n -octyl acetate in the presence of CBr 4 ·2AlBr 3 followed by treatment with nucleophiles such as alcohols, amines or (het)arenes affords 7-acetoxy-2,2-dimethylheptanoyl-containing products.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b08b3ed5206da2c6bd79f48ae0c238b
https://doi.org/10.1016/j.mencom.2011.11.010
https://doi.org/10.1016/j.mencom.2011.11.010
Autor:
E. I. Goryunov, Lyudmila V. Afanas’eva, Nikolai D. Kagramanov, Irena S. Akhrem, I. M. Churilova, Pavel V. Petrovskii, Dzhul’etta V. Avetisyan
Publikováno v:
Mendeleev Communications. 21:259-261
Treatment of 1-bromoadamantane and 1-bromo-3,5-dimethyladamantane with CBr 4 ·2AlBr 3 under carbon monoxide atmosphere followed by quenching with nucleophiles affords 1,3-dicarbonyl adamantanes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2cd42f535161c4066d31d032aa4d92a
https://doi.org/10.1016/j.mencom.2011.09.009
https://doi.org/10.1016/j.mencom.2011.09.009