Zobrazeno 1 - 10
of 27
pro vyhledávání: '"N. N. Yusubov"'
Publikováno v:
Russian Journal of General Chemistry. 90:1447-1452
Alcoholysis of α-chloro-α-phosphonopropionic acid trichloride with allyl and propargyl alcohols was studied. It was found that the reaction proceeded selectively at the carbonyl carbon atom. The reaction of α-chloro-α-phosphonopropionic acid tric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::03a209f2a1957248eba510b6c20c92f1
https://doi.org/10.1134/s1070363220080113
https://doi.org/10.1134/s1070363220080113
Publikováno v:
Russian Journal of General Chemistry. 90:89-92
Addition of ethanol and diethyl phosphonate to the carbonyl group of 2,2-dichloro-2-(diethoxyphosphoryl)-acetaldehyde has been studied, and the corresponding α-chloro ether, acetal, and phosphorylated metrifonate have been obtained. α,α-Dichloro-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::01175f066fb95e279eb6d1cc4e4b66f1
https://doi.org/10.1134/s1070363220010132
https://doi.org/10.1134/s1070363220010132
Autor:
N. N. Yusubov, N. D. Sadikhova, G. E. Allakhverdiyeva, B. M. Ismailov, A. R. Mamedbeyli, G. G. Ibragimova, I. A. Mamedov
Publikováno v:
Russian Journal of General Chemistry. 89:1394-1397
The alkylation reactions of phosphonoacetic aldehyde and ethyl phosphonoacetate with ethyl α-bromopropanoate in DMSO in the presence of K2CO3 have been studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abfa061bed14ba3056bcdcbf123955ad
https://doi.org/10.1134/s1070363219070077
https://doi.org/10.1134/s1070363219070077
Alkylation of methylene-active compounds with halo acetals and hydrolysis of the alkylation products
Autor:
I. A. Mamedov, N. N. Yusubov, N. D. Sadykhova, G. G. Ibragimova, R. A. Gasymov, V. M. Ismailov
Publikováno v:
Russian Journal of Organic Chemistry. 52:1390-1393
A preparative procedure has been proposed for the alkylation of CH acids with halo acetals and hydrolysis of the alkylation products to furan derivatives and lactones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e062ae6e032354300da7ba52ad0b972
https://doi.org/10.1134/s1070428016100031
https://doi.org/10.1134/s1070428016100031
Autor:
N. D. Sadykhova, F. N. Nagiev, G. G. Ibragimova, N. N. Yusubov, V. M. Ismailov, I. A. Mamedov
Publikováno v:
Russian Journal of Organic Chemistry. 53:1099-1101
Alkylation of methyl 4-chloro-3-oxobutanoate with 1,2-dibromoethane, 1,3-dibromopropane, and 1,2,3-tribromopropane afforded the corresponding dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate enol ethers.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::468ac9c1a6df5e9a9d56fc41a567909a
https://doi.org/10.1134/s1070428017070247
https://doi.org/10.1134/s1070428017070247
Publikováno v:
Russian Journal of Organic Chemistry. 53:950-952
The alkylation of dimethyl 3-oxopentanedioate with 1,2-dibromoethane and 1,2,3-tribromopropane afforded C,C-(cyclopropane derivative) and C,O-dialkylation products. The initial trioxo compound underwent partial self-condensation to produce resorcinol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7ead2e936233cc2105dbf552ff92770f
https://doi.org/10.1134/s1070428017060239
https://doi.org/10.1134/s1070428017060239
Publikováno v:
Russian Journal of General Chemistry. 86:1630-1632
Reactions of trichloride of phosphono carboxylic acid with β-dicarbonyl compounds proceed at the active methylene group with the formation of the С-acylation product with a small admixture of the product of O-acylation. The C-acylation products und
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e33465d23c1517f1443d1c076f58a97d
https://doi.org/10.1134/s1070363216070161
https://doi.org/10.1134/s1070363216070161
Publikováno v:
Russian Journal of Applied Chemistry. 81:323-325
Free-radical cooligomerization of a new polyfunctional monomer, p-isopropenylphenyl λ-chlorobutyrate, with styrene was studied.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::102bdad04b64b7f0be3064e30a807c52
https://doi.org/10.1134/s1070427208020328
https://doi.org/10.1134/s1070427208020328
Publikováno v:
ChemInform. 44
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe57105250114b6e5bf7f45b792c8c94
https://doi.org/10.1002/chin.201350087
https://doi.org/10.1002/chin.201350087
Autor:
N. N. Yusubov
Publikováno v:
Russian Chemical Bulletin. 45:1433-1436
The reactions of (ω)-alkylthioalkyl)phenols with formaldehyde and secondary amines afforded the corresponding aminomethyl derivatives, in which the dimethylamino group may be replaced by the alkylthio group.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ca092cc74af733665c4662130e252ba
https://doi.org/10.1007/bf01434227
https://doi.org/10.1007/bf01434227