Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Yu. O. Subbotina"'
Publikováno v:
Russian Journal of General Chemistry. 85:1629-1634
The effect of fluorine atoms in the benzene ring on the photophysical properties of 2-methyl-6,7-difluoro-8-hydroxyquinoline is studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adba6692e46fe582718bcd13102edf00
https://doi.org/10.1134/s1070363215070099
https://doi.org/10.1134/s1070363215070099
Autor:
Pavel A. Slepukhin, G. L. Rusinov, Valery N. Charushin, Yu. O. Subbotina, Egor V. Verbitskiy, Ekaterina M. Cheprakova, M. S. Valova, Alexander V. Schepochkin
Publikováno v:
Chemistry of Heterocyclic Compounds. 50:814-827
Novel organic dyes containing pyridine ring as the anchoring group with carbazole or triphenylamine substituents were synthesized from available 4-(2-thienyl)pyrimidine using the Kost–Sagitullin rearrangement and Suzuki cross coupling assisted by m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::050e9458e5e55f3ff1f794baef1b56e5
https://doi.org/10.1007/s10593-014-1536-x
https://doi.org/10.1007/s10593-014-1536-x
Publikováno v:
Russian Journal of General Chemistry. 84:486-495
In order to comprehend the data on reactivity of polychlorinated biphenyls of the Sovol mixture in nucleophilic substitution reactions we have performed quantum-chemical simulation using the RB3LYP\6-31G(d) gas phase approximation. Using the “Atoms
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c67cd4eebd38e9b9e8d1277f1559123f
https://doi.org/10.1134/s107036321403013x
https://doi.org/10.1134/s107036321403013x
Publikováno v:
Chemistry of Heterocyclic Compounds. 39:1504-1515
The cyclization of 1,3,5-hexatrien-1-one, 1, and the Z- and E-isomers of 1-aza-1,3-butadienylketene 3 were studied using the semiempirical AM1 and PM3 methods. Cyclizations of compounds 1 and Z-3 are shown to occur via a mono-rotation mechanism with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6b7ed63130a7b6af183e4e999750b9a
https://doi.org/10.1023/b:cohc.0000014416.75284.9d
https://doi.org/10.1023/b:cohc.0000014416.75284.9d
Autor:
Yu. G. Budnikova, Alexander V. Shchepochkin, Yu. O. Subbotina, O. N. Chupakhin, V. N. Charushin, G. L. Rusinov, Pavel A. Slepukhin
Publikováno v:
Russian Chemical Bulletin
A reaction of NH-heterocycles with the 10-methylacridinium cation in the presence of a base led to 9,10-dihydro-10-methyl-9-substituted acridines, which can be considered as stable intermediates in the aromatic nucleophilic substitution reaction of h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bb8919baaf656102fa5ba461fbb7481
https://hdl.handle.net/10995/27419
https://hdl.handle.net/10995/27419
Publikováno v:
ChemInform. 31
8-Vinyl-, styryl-, (l-propenyl)thioquinolines, 8-quinoline vinyl sulfoxide, and 8-quinoline vinyl sulfone have been synthesized. Their structures have been studied by molecular mechanics and quantum chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cbd7f3d9101ead4cca40ecde12a5fab
https://doi.org/10.1002/chin.200036151
https://doi.org/10.1002/chin.200036151
Publikováno v:
ChemInform. 36
A selective procedure was developed for the synthesis of 1,2,3-triazoles and unsymmetrically substituted diazomalonamides. Cyclization of unsymmetrically substituted diazomalonamides to 1,2,3-triazoles was studied by the method of intramolecular comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40f13fab99c756bd6701979709fbb9ad
https://doi.org/10.1002/chin.200509120
https://doi.org/10.1002/chin.200509120
Publikováno v:
Russian Chemical Bulletin; Jun2004, Vol. 53 Issue 6, p1305-1310, 6p
Publikováno v:
Scopus-Elsevier
8-Vinyl-, styryl-, (l-propenyl)thioquinolines, 8-quinoline vinyl sulfoxide, and 8-quinoline vinyl sulfone have been synthesized. Their structures have been studied by molecular mechanics and quantum chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81553b48cf0a52b35c201786c04a0396
http://www.scopus.com/inward/record.url?eid=2-s2.0-27544497961&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-27544497961&partnerID=MN8TOARS