Zobrazeno 1 - 10 of 19 pro vyhledávání: '"T I, Guseva"'
1
Cyanoacrylate-based adhesives
Autor: N. G. Senchenya, Yu. G. Gololobov, T. I. Guseva
Publikováno v: Polymer Science Series C. 49:235-239
The effect the curing conditions on the properties of adhesive joints formed using cyanoacrylate-based adhesives is investigated. The temperature dependences of relative rigidity and mechanical loss tangent are studied by torque analysis for poly(eth
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2c78bf17db3b7d72bd77bd6b0b36de5a
https://doi.org/10.1134/s181123820703006x
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2
[Untitled]
Autor: N. G. Senchenya, T. I. Guseva, Pavel V. Petrovskii, Yu. G. Gololobov
Publikováno v: Russian Chemical Bulletin. 50:838-842
The reactions of mono- and bis-isocyanates with bis-carbanions whose COOAlk groups at the anionic centers do not contain acidic hydrogen atoms proceed unusually to form bis-carbamates (including oligomeric carbamates) due to migration of the alkoxyca
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::21caccb2986af4a24ce7ec17131fd04b
https://doi.org/10.1023/a:1011355008917
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3
[Untitled]
Autor: T. I. Guseva, N. G. Sencheniya, Boris Tumanskii, I. R. Golding, R. G. Gasanov
Publikováno v: Russian Chemical Bulletin. 50:2356-2359
The rate constants for the addition of ·CH(Ph)CH2CCl3, ·CH2Ph, ·CH2Prn, and ·CCl3 radicals to the ethyl 2-cyanoacrylate molecule were determined by ESR spectroscopy using the spin trapping technique.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f35e9434da965da7bc75884b49ae65a4
https://doi.org/10.1023/a:1015075227538
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4
Electrophilic 1,3-C→N− and-N→C− migrations in saturated systems
Autor: N. G. Senchenya, M. A. Galkina, T. I. Guseva, Yu. G. Gololobov, I. Yu. Kuz'mintseva, O. V. Dovgan, Pavel V. Petrovskii
Publikováno v: Russian Chemical Bulletin. 48:1622-1627
A new type of intramolecular electrophilic rearrangements involving the shift of COOAlk groups from carbon to an N-anionic center is considered. Carbanionic species with COOAlk groups at anionic centers containing no acidic hydrogen react unusually w
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e686519093a0ca94388d43cad1dea1aa
https://doi.org/10.1007/bf02494803
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5
Synthesis of functionally substituted 2-cyanoacrylates
Autor: T. I. Guseva, Yu. G. Gololobov, V. A. Tsyryapkin, N. G. Senchenya, K. A. Mager
Publikováno v: Russian Chemical Bulletin. 43:595-598
The conditions for the Knoevenagel synthesis of 2-cyanoacrylates containing double and triple bonds in the alkoxycarbonyl group have been studied. It was found that the esters are formed in 10–70 % yields by the condensation of the respective cyano
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::20e0303bfe814b37fc2078964c6b8909
https://doi.org/10.1007/bf00699831
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7
ChemInform Abstract: Reaction of α-Cyanoacrylates with Functionally-Substituted Thiols, Ethanedithiol, and Hydrogen Sulfide
Autor: I. O. Bragina, T. I. Guseva, B. D. Lavrukhin, I. I. Kandror, Yu. G. Gololobov, M. A. Galkina
Publikováno v: ChemInform. 25
Functionally substituted thiols, i.e., thioglycolic acid and cysteamine and cysteine hydrochlorides, facilely undergo addition at the double bond of α-cyanoacrylates, forming the corresponding adducts in quantitative yields: R′SCH2CH(CN)COOR [R′
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5ed7214e8194bc01d4b4f5dac749e62d
https://doi.org/10.1002/chin.199402134
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8
ChemInform Abstract: Electrophilic 1,3-C→N- and -N→C- Migrations in Saturated Systems
Autor: I. Yu. Kuz'mintseva, T. I. Guseva, N. G. Senchenya, M. A. Galkina, O. V. Dovgan, Pavel V. Petrovskii, Yu. G. Gololobov
Publikováno v: ChemInform. 31
A new type of intramolecular electrophilic rearrangements involving the shift of COOAlk groups from carbon to an N-anionic center is considered. Carbanionic species with COOAlk groups at anionic centers containing no acidic hydrogen react unusually w
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5bfcf5cecd324ab2550b99f63f6fd201
https://doi.org/10.1002/chin.200011260
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9
ChemInform Abstract: Intramolecular Electrophilic Rearrangements in Saturated Acyclic Systems. Reactions of Bis-carbanions with Isocyanates
Autor: Yu. G. Gololobov, Pavel V. Petrovskii, T. I. Guseva, N. G. Senchenya
Publikováno v: ChemInform. 33
The reactions of mono- and bis-isocyanates with bis-carbanions whose COOAlk groups at the anionic centers do not contain acidic hydrogen atoms proceed unusually to form bis-carbamates (including oligomeric carbamates) due to migration of the alkoxyca
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d49d7270edb30cb867fe6fe36700f9b3
https://doi.org/10.1002/chin.200201049
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10
Reaction of ?-cyanoacrylates with functionally substituted thiols, ethanedithiol, and hydrogen sulfide
Autor: I. I. Kandror, I. O. Bragina, M. A. Galkina, B. D. Lavrukhin, Yu. G. Gololobov, T. I. Guseva
Publikováno v: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science. 40:2456-2459
Functionally substituted thiols, i.e., thioglycolic acid and cysteamine and cysteine hydrochlorides, facilely undergo addition at the double bond of α-cyanoacrylates, forming the corresponding adducts in quantitative yields: R′SCH2CH(CN)COOR [R′
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::435203b557c24b44f59c65dee5d83c0d
https://doi.org/10.1007/bf00959721
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