Zobrazeno 1 - 10
of 20
pro vyhledávání: '"V. Mezhnev"'
Autor:
J. Y. Sanchez, E. G. Bulycheva, V. Yu. Voitekunas, A. E. Osolodkov, Mikhail D. Dutov, Svyatoslav A. Shevelev, Marc J.M. Abadie, Olga V. Serushkina, Cristina Iojoiu, A. L. Rusanov, Vasily V. Mezhnev, M. P. Prigozhina, L. G. Komarova, M. G. Bugaenko
Publikováno v:
Polymer Science Series B. 51:465-470
New poly(arylene ethers) containing side sulfo groups have been synthesized through the copolycondensation of 3,5-dinitrodiphenyl sulfone 4′-sulfonic acid and 4,4′-dichlorodiphenyl sulfone with bicyclic aromatic bisphenols under the conditions of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3c077cb401e55a40e3efe1000858902
https://doi.org/10.1134/s1560090409110074
https://doi.org/10.1134/s1560090409110074
Publikováno v:
Russian Chemical Bulletin. 54:1048-1051
Conditions were found under which 2,4,6-trinitrostyrene derived from 2,4,6-trinitrotoluene adds nucleophiles (thiophenol, aniline, and aliphatic amines) at the vinyl fragment to form the corresponding β-X-ethyl-2,4,6- trinitrobenzenes (X = PhS, PhNH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc36f1fc28c2df9435702bc689c56440
https://doi.org/10.1007/s11172-005-0357-6
https://doi.org/10.1007/s11172-005-0357-6
Autor:
V. V. Mezhnev, R. Ch. Geivandov
Publikováno v:
Russian Chemical Bulletin. 60:2114-2116
Cyclization of 2-(4-bromophenyl)-5-pentylcyclohex-1-ene-1-carboxylic acid followed by reduction of the carbonyl group resulted in the corresponding 7-substituted derivative of 2-alkyl-2,3,4,9-tetrahydro-1H-fluorene.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e8e5061091af135c7f600f9fde1f3af
https://doi.org/10.1007/s11172-011-0325-2
https://doi.org/10.1007/s11172-011-0325-2
Publikováno v:
Russian Chemical Bulletin. 59:662-664
Reactions of nucleophiles with 3-R-4, 6-dinitrobenzo[c]isoxazoles (anthranils) were studied. Reactions of 4, 6-dinitroanthranil (R = H) with anionic O- and S-nucleophiles (phenols and benzenethiols in the presence of K2CO3) do not result in displacem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f20aa91778c70fdbbf4373f1fe1b63bb
https://doi.org/10.1007/s11172-010-0128-x
https://doi.org/10.1007/s11172-010-0128-x
Publikováno v:
Russian Chemical Bulletin. 58:476-478
A preparative method for the synthesis of 4,6-dinitroanthranil by intramolecular cyclization of 2-azido-4,6-dinitrobenzaldehyde was developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ea2771247cd178364bda40a7fd3cefa
https://doi.org/10.1007/s11172-010-0036-0
https://doi.org/10.1007/s11172-010-0036-0
Publikováno v:
Letters in Organic Chemistry. 5:202-204
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::988a84cf3046dc220ecc03b4e144e1f0
https://doi.org/10.2174/157017808783955907
https://doi.org/10.2174/157017808783955907
Autor:
V. V. Mezhnev, R. Ch. Geivandov
Publikováno v:
ChemInform. 43
A facile synthetic approach towards hitherto unknown fluorene derivatives, key intermediates for the preparation of a novel class of liquid crystals, is presented.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2bd2f300a699a4064a908db9a585336
https://doi.org/10.1002/chin.201247085
https://doi.org/10.1002/chin.201247085
Publikováno v:
ChemInform. 41
Starting from TNT, a novel access to 4,6-dinitrobenzo[c]isoxazole (III) is developed and compared with other synthetic strategies.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ba7d1a0b8fc8d385c713fe7ad46bff4c
https://doi.org/10.1002/chin.201036130
https://doi.org/10.1002/chin.201036130
Publikováno v:
ChemInform. 39
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0aab204903affb340739e3089c3a08eb
https://doi.org/10.1002/chin.200831141
https://doi.org/10.1002/chin.200831141
Autor:
V. V. Mezhnev, Oleg Yu. Sapozhnikov, Mikhail D. Dutov, Svyatoslav A. Shevelev, Vadim V. Kachala
Publikováno v:
ChemInform. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83614f255d435d6c202600bac965b560
https://doi.org/10.1002/chin.200748130
https://doi.org/10.1002/chin.200748130