Zobrazeno 1 - 10
of 19
pro vyhledávání: '"T. A. Yangirov"'
Autor:
T. A. Yangirov, N. G. Gileva, A. A. Fatykhov, E. S. Meshcheryakova, L. M. Khalilov, V. A. Kraikin
Publikováno v:
Russian Journal of Organic Chemistry. 58:1254-1259
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a7b380c6765e51df698ef65131e9e3d
https://doi.org/10.1134/s1070428022090093
https://doi.org/10.1134/s1070428022090093
Publikováno v:
Russian Journal of General Chemistry. 92:996-1004
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e8f30f35a986646d094198600ac7bd4
https://doi.org/10.1134/s1070363222060111
https://doi.org/10.1134/s1070363222060111
Autor:
T. A. Yangirov, B. M. Abdullin, A. A. Fatykhov, R. Kh. Yumagulova, A. R. Ayupova, V. A. Kraikin
Publikováno v:
Russian Chemical Bulletin. 70:1804-1815
The thermal polymerization of styrene in the presence of polymer initiators, copoly(arylene phthalides) of the diphenyl oxide series with different ratios of two adjacent (“head-to-head”) and single (“head-to-tail”) phthalide groups, was stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6248a9fe367c216c5080587040a0e0e2
https://doi.org/10.1007/s11172-021-3286-0
https://doi.org/10.1007/s11172-021-3286-0
Autor:
B. M. Abdullin, E. M. Zakharova, T. A. Yangirov, Sergey N. Salazkin, A. A. Fatykhov, V. A. Kraikin
Publikováno v:
Polymer Science, Series B. 63:13-21
The interbicopolycondensation of 3,3'-bis(4-phenoxyphenyl)-3,3'-diphthalide and diphenyl oxide with intermonomer, 4,4'-bis(2-carboxybenzoyl)diphenyl oxide pseudoacid dichloride, proceeding by the Friedel–Crafts electrophilic substitution mechanism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::062fe2308a91b7c22025ebf6344fe796
https://doi.org/10.1134/s1560090421010085
https://doi.org/10.1134/s1560090421010085
Publikováno v:
Izvestia Ufimskogo Nauchnogo Tsentra RAN. :117-120
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1b793742440693df13d41c066171d07
https://doi.org/10.31040/2222-8349-2019-0-4-117-120
https://doi.org/10.31040/2222-8349-2019-0-4-117-120
Publikováno v:
Izvestia Ufimskogo Nauchnogo Tsentra RAN. :98-101
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69ea696ae4d27171b1dd495627572c93
https://doi.org/10.31040/2222-8349-2019-0-4-98-101
https://doi.org/10.31040/2222-8349-2019-0-4-98-101
Autor:
N. G. Gileva, A. A. Fatykhov, T. A. Yangirov, E. A. Sedova, R. R. Khafizova, E. S. Meshcheryakova, V. A. Kraikin, Leonard M. Khalilov
Publikováno v:
Russian Journal of Organic Chemistry. 55:670-677
A new protocol of the synthesis of 3,3′-diaryl-3,3′-diphthalides by dehalogenation of o-keto carboxylic acid pseudochlorides is implemented. The feature of the new protocol is that the reaction is carried out in the presence of a zero-valent nick
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d30a9653642d9ce29d1bbd2c3474ad2
https://doi.org/10.1134/s1070428019050142
https://doi.org/10.1134/s1070428019050142
Autor:
V. A. Kraikin, Sergey N. Salazkin, T. A. Yangirov, A. A. Fatykhov, Leonard M. Khalilov, E. S. Meshcheryakova, E. A. Sedova, Sergey P. Ivanov
Publikováno v:
Tetrahedron. 75:1282-1292
A wide range of diastereomeric pairs of biaryl-3,3′-diphthalides with aromatic (heteroaromatic) substituents of polyphenylene series (including halogen substituted) was synthesized. All of them were separated and characterized by the methods of X-r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a25f7c5e905dceaedc2aae0d59287687
https://doi.org/10.1016/j.tet.2019.01.043
https://doi.org/10.1016/j.tet.2019.01.043
Autor:
Rimma M. Sultanova, Mikhail Ovchinnikov, T. A. Yangirov, Sergey L. Khursan, Alexander N. Lobov
Publikováno v:
The Journal of Physical Chemistry B. 121:6601-6609
The effect of Lewis base (LB) in the domino reaction between methyl diazoacetate and methyl acrylate has been studied. This domino process is initialized by a [3+2]-cycloaddition reaction to generate 3H-pyrazoline followed by a subsequent 1,3-H-shift
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::820c7753930d8612d5466b0d024e1ab6
https://doi.org/10.1021/acs.jpcb.7b02064
https://doi.org/10.1021/acs.jpcb.7b02064
Autor:
V. A. Kraikin, A. A. Fatykhov, Valentina P Ivanova, Natalia G Gileva, E. A. Sedova, Irina A. Ionova, T. A. Yangirov
Publikováno v:
High Performance Polymers. 29:677-690
The polyheteroarylenes of new type, called polyarylenediphthalides (PADPs), containing two adjacent phthalide groups regularly alternating with aromatic (heteroaromatic) fragments in the main chain have been developed. For obtaining PADPs, two approa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::091609cc869b382d5e1d68bdab0977cf
https://doi.org/10.1177/0954008317698031
https://doi.org/10.1177/0954008317698031