Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Mukattis B. Gazizov"'
Autor:
Sona A. Agadzhanyan, Mukattis B. Gazizov, Larisa P. Shamsutdinova, Olga A. Stokolos, David R. Aleksanyan, Karina G. Aleksanyan, Alena S. Sorokina, Anastasia L. Pistsova, Vladimir N. Koshelev, Anastasia Yu. Kilyakova, Eduard G. Cheban
Publikováno v:
IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENII KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA. 64:35-43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eeee762f943e7d60db3b3a5a0fd2fd4b
https://doi.org/10.6060/ivkkt.20216411.6476
https://doi.org/10.6060/ivkkt.20216411.6476
Autor:
Yu. S. Kirillina, Rafail A. Khairullin, Mukattis B. Gazizov, L. P. Shamsutdinova, S. Yu. Ivanova
Publikováno v:
Russian Journal of General Chemistry. 90:84-88
The adduct of O, O-dialkyldithiophosphoric acid and enamine reacts exothermically with an electrophilic reagent. In the case of sulfenyl bromide, the iminium salt reduced at the C-Br bond and bis(dialkoxythiophosphorylthio)-disulfide have been formed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f51aea2c4e9fbbad65f9755bfed7fbb4
https://doi.org/10.1134/s1070363220010120
https://doi.org/10.1134/s1070363220010120
Autor:
S. Yu. Ivanova, G. D. Valieva, K. S. Gazizova, Mukattis B. Gazizov, R. F. Karimova, Rafail A. Khairullin
Publikováno v:
Russian Journal of General Chemistry. 89:2386-2389
S-Methyl diethylphosphinothioate reacted with benzylidene chlorides to give the corresponding aryl(chloro)methyl methyl sulfide and diethylphosphinoyl chloride. The product structure suggests initial attack of the methylsulfanyl group on the CH carbo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::551f8690834b2678de95caedf308d116
https://doi.org/10.1134/s1070363219120107
https://doi.org/10.1134/s1070363219120107
Mono- and Di(dechloromethylthioylation) of Dichloromethylarenes with S-Methyl Diethylthiophosphinate
Autor:
Igor S. Antipin, Mukattis B. Gazizov, Yu. S. Kirillina, Rafail A. Khairullin, S. Yu. Ivanova, G. D. Valieva
Publikováno v:
Doklady Chemistry. 489:257-260
The attack of the thiol sulfur atom (P–SMe) on the methine carbon as the main route of the new reaction of dichloromethylarenes with S-methyl diethylthiophosphinate has been predicted and experimentally confirmed on the basis of the electronic stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a39dbc4f21b9beceec3042b14f592686
https://doi.org/10.1134/s0012500819110016
https://doi.org/10.1134/s0012500819110016
Autor:
K. S. Gazizova, O. D. Khairullina, Mukattis B. Gazizov, S. Yu. Ivanova, Yu. S. Kirillina, Rafail A. Khairullin
Publikováno v:
Russian Journal of General Chemistry. 89:2178-2184
Acyclic phthalaldehyde diacetal without cyclic 1,3-dihydro-1,3-dimethoxybenzo[c]furan impurity has been obtained via the reaction of 1,2-bis(dibromomethyl)benzene with trimethyl orthoformate (1:6) at 90°C in the presence of 10 mol% of ZnCl2. Hydroly
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d70a7938d6a23cba43c9b9e3b999c14f
https://doi.org/10.1134/s1070363219110021
https://doi.org/10.1134/s1070363219110021
Autor:
Rafail A. Khairullin, A. L. Pistsova, O. D. Khairullina, Sh. N. Ibragimov, Mukattis B. Gazizov, Yu. S. Kirillina, K. S. Gazizova, S. Yu. Ivanova
Publikováno v:
Russian Journal of General Chemistry. 89:63-66
[4-(Diethylamino)phenyl]dichlorophosphine synthesized for the first time has reacted with trialkyl orthoformate and ethylene oxide in the presence of ethyl chloroacetate with the formation of phosphorylated formals and ethyl [4-(diethylamino)phenyl](
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c8e8d740b9ddd0b30c39e63076fd190a
https://doi.org/10.1134/s1070363219010110
https://doi.org/10.1134/s1070363219010110
Publikováno v:
Russian Journal of General Chemistry. 88:2243-2250
A new procedure has been developed for the simultaneous preparation of terephthalaldehyde and 4-(dibromomethyl)benzaldehyde by catalytic debromophosphoryl- and phosphonyloxylation of 1,4-bis- (dibromomethyl)benzene with P(IV) acid methyl esters. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::85752455ada6f2ba04edbb8e7867b705
https://doi.org/10.1134/s1070363218110014
https://doi.org/10.1134/s1070363218110014
Publikováno v:
Russian Journal of General Chemistry. 88:2079-2083
Effect of the substituent on the imine carbon atom on the result of the reaction of P(IV) dithio acids with N-Alkyl-α-chloroketimines has been studied. New types of ketones containing (O,O-diisopropyl phosphorothioyl)sulfanyl and (diphenylphosphinot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::41a6d73e364a2a2bd45c9e6586066cb4
https://doi.org/10.1134/s1070363218100080
https://doi.org/10.1134/s1070363218100080
Autor:
N. N. Gazizova, Sh. N. Ibragimov, S. Yu. Ivanova, N. Yu. Bashkirtseva, Rafail A. Khairullin, A. D. Kostenko, Mukattis B. Gazizov
Publikováno v:
Russian Journal of General Chemistry. 87:2783-2788
Reactions of 4-(dibromomethyl)benzaldehyde with trialkyl orthoformates in the presence of both Bronsted (H2SO4) and Lewis (ZnCl2) acids involved acetalization of the aldehyde group. In the first case, the corresponding acetal is formed as the only pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a3b55ff2952deab7cd219cde95f321d
https://doi.org/10.1134/s1070363217120052
https://doi.org/10.1134/s1070363217120052
Autor:
N. S. Tikhonova, L. P. Shamsutdinova, A. L. Pistsova, R. N. Burangulova, Mukattis B. Gazizov, R. F. Karimova, R. K. Ismagilov
Publikováno v:
Russian Journal of General Chemistry. 87:2891-2894
The addition of thioacetic acid to 2,6-di-tert-butyl-4-(phosphorylmethylidene)cyclohexa-2,5-dien-1-ones has been accomplished for the first time. The resulting adduct is readily hydrolyzed with hydrazine hydrate to give 2,6-di-tert-butyl-4-[phosphory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::34671e08896e5256ab3de77a164eae32
https://doi.org/10.1134/s1070363217120246
https://doi.org/10.1134/s1070363217120246