Zobrazeno 1 - 10 of 29 pro vyhledávání: '"R I Aminov"'
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Synthesis of Polycyclic Hydrocarbons C14H20 by Hydrogenation of exo–exo-, exo–endo-, endo–exo-, and endo–endo-Hexacyclo[9.2.1.02,10.03,8.04,6.05,9]tetradec-12-enes with H2SO4 and Isomerization of the Products to Diamantane Induced by Ionic Liquids
Autor: R. I. Aminov, Ravil I. Khusnutdinov
Publikováno v: Industrial & Engineering Chemistry Research. 60:12776-12782
A new method was developed for hydrogenation of unsaturated hexacyclic norbornadiene dimers, exo-exo-, exo-endo-, endo-exo-, and endo-endo- hexacyclo[9.2.1.02,10.03,8.04,6.05,9]tetradec-12-enes, using sulfuric acid (98%), giving pentacyclo[8.2.1.15,8
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::51fa2658def33ad9955718183007162c
https://doi.org/10.1021/acs.iecr.1c02082
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3
A new method for the synthesis of diamantane by hydroisomerization of binor-S on treatment with sulfuric acid
Autor: Ravil I. Khusnutdinov, R. I. Aminov
Publikováno v: Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 16, Iss 1, Pp 2534-2539 (2020)
A new method was developed for the direct synthesis of the second representative of the homologous series of diamond-like hydrocarbons, diamantane, in 65% yield by hydroisomerization of the norbornadiene dimer, endo-endo-heptacyclo[8.4.0.02,12.03,8.0
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a9d78003f93e3468c655b644f679a88
http://europepmc.org/articles/PMC7588729
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4
Reactions of Binor-S with α,ω-Diols and Organic Acids in the Presence of Inorganic Ionic Liquids
Autor: R. I. Aminov, I. M. Karimova, R. I. Khusnutdinov
Publikováno v: Russian Journal of Organic Chemistry. 56:1595-1599
New methods have been developed for the synthesis of previously unknown ω-(hexacyclo[9.2.1.02,7.03,5.04,8.09,13]tetradecan-10-exo-yloxy)alkan-1-ols and hexacyclo[9.2.1.02,7.03,5.04,8.09,13]tetradecan-10-exo-yl carboxylates by reactions of heptacyclo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1c5db78b1722bfdae17c706611d33cdb
https://doi.org/10.1134/s1070428020090158
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5
Iron(III) chloride promoted Ritter amidation of saturated cyclopropane-containing polycyclic hydrocarbons
Autor: R. I. Aminov, Leonard M. Khalilov, Ekaterina S. Mescheryakova, Ravil I. Khusnutdinov, Tatyana M. Egorova
Publikováno v: Mendeleev Communications. 30:369-371
The Ritter-type amidation of cyclopropane-containing norbornane hydrocarbons proceeds via cyclopropane ring opening upon treatment with aceto- or propionitrile and water in the presence of FeCl3·6 H2O as a catalyst.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2d8c76a9d5006bba35311be179bf8223
https://doi.org/10.1016/j.mencom.2020.05.036
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6
Benzene Alkylation with Cycloolefins under the Action of [Et3NH]+[Al2Cl7]− Ionic Liquid
Autor: Ravil I. Khusnutdinov, A. S. Mazitova, R. I. Aminov
Publikováno v: Russian Journal of General Chemistry. 89:2171-2177
Benzene alkylation with mono- and bicyclic olefins under the action of an inorganic ionic liquid [Et3NH]+[Al2Cl7]− with the formation of benzene cycloalkyl derivatives in 58–98% yield has been performed for the first time. It has been found that
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::43d0a9c24892f8cd91a487a6e321eb15
https://doi.org/10.1134/s107036321911001x
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7
Alcoholysis of Binor-S with Alcohols under the Action of Ionic Liquid
Autor: R. I. Aminov, Ravil I. Khusnutdinov
Publikováno v: Russian Journal of Organic Chemistry. 55:587-591
Inorganic ionic liquids are first shown to catalyze the alcoholysis of heptacyclo-[8.4.0.02,12.03,8.04,6.05,9.011,13]tetradecane (heptacyclic dimer of norbornadiene, binor-S) with primary and secondary alcohols. The reaction occurs at 65−100°C for
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::994c5275d29dab85bff48972f34939a7
https://doi.org/10.1134/s1070428019050014
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8
Synthesis of polycyclic hydrocarbons C14H20 by hydrogenation of exo-exo-, exo-endo-, endo-exo-, and endo-endo- hexacyclo[9.2.1.02,10.03,8.04,6.05,9]tetradec-12-enes with H2SO4 and isomerization of the products to diamantane induced by ionic liquids
Autor: R. I. Aminov, Ravil I. Khusnutdinov
A new method was developed for hydrogenation of unsaturated hexacyclic norbornadiene dimers, exo-exo-, exo-endo-, endo-exo-, and endo-endo- hexacyclo[9.2.1.02,10.03,8.04,6.05,9]tetradec-12-enes, using sulfuric acid (98%), giving pentacyclo[8.2.1.15,8
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3e4b7822563df646dac6a4e1738a595e
https://doi.org/10.3762/bxiv.2021.24.v1
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10
Quinolines synthesis by reacting 1,3-butanediol with anilines in the presence of iron catalysts
Autor: Ravil I. Khusnutdinov, R. I. Aminov, A. R. Bayguzina
Publikováno v: Russian Journal of General Chemistry. 86:1613-1618
2-, 4-, 6-, 7-, and 8-substituted quinolines were synthesized in 78–95% yield by the reaction of 1,3- butanediol with anilines in the presence of iron catalysts in carbon tetrachloride.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::147df9a1507c579e0be676581d7b249a
https://doi.org/10.1134/s1070363216070136
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