Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Liudmila L. Rodina"'
Autor:
Liudmila L. Rodina, Xenia V. Azarova, Jury J. Medvedev, Dmitrij V. Semenok, Valerij A. Nikolaev
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2250-2258 (2018)
The sensitized photoexcitation of 2-diazocyclopentane-1,3-diones in the presence of THF leads to the insertion of the terminal N-atom of the diazo group into the α-С–Н bond of THF, producing the associated N-alkylhydrazones in yields of up to 63
Externí odkaz:
https://doaj.org/article/676c9dc824c94b58807eadbc3db09d14
Autor:
Dmitrij V Semenok, Jury J. Medvedev, Valerij A. Nikolaev, Liudmila L. Rodina, Xenia V. Azarova
Publikováno v:
Beilstein Journal of Organic Chemistry
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2250-2258 (2018)
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2250-2258 (2018)
The sensitized photoexcitation of 2-diazocyclopentane-1,3-diones in the presence of THF leads to the insertion of the terminal N-atom of the diazo group into the α-С–Н bond of THF, producing the associated N-alkylhydrazones in yields of up to 63
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9968a066627c1cf1fc3ca3a44a727370
https://doi.org/10.3762/bjoc.14.200
https://doi.org/10.3762/bjoc.14.200
Autor:
Liudmila L. Rodina, Nina L. Tonogina, Victor I. Baranovskii, Valerij A. Nikolaev, Alexey Povolotskiy, Olesia S. Galkina
Publikováno v:
The Journal of Organic Chemistry. 82:11399-11405
The energies and lifetimes of the excited states (S1, S2, S5, T1) of a diazotetrahydrofuranone were determined using experimental and computational methods. It was shown that direction of the diazoketone photochemical transformations without eliminat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65b613d0adabd5da4559d0941f71aa45
https://doi.org/10.1021/acs.joc.7b01848
https://doi.org/10.1021/acs.joc.7b01848
Autor:
Xenia V. Azarova, Dmitrii V. Semenok, Jury J. Medvedev, Liudmila L. Rodina, Valerij A. Nikolaev
Publikováno v:
Synthesis. 48:4525-4532
The interaction of 5,5-dialkyl(diaryl)-substituted 4-diazo-3(2H)furanones with Bronsted acids (TFA, TsOH, etc.) causes elimination of nitrogen accompanied by 1,2-nucleophilic rearrangement, giving rise to exclusive formation of 4,5-dialkyl(diaryl)-su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d5d4f509e6fc09802122409bd3a04da
https://doi.org/10.1055/s-0036-1588304
https://doi.org/10.1055/s-0036-1588304
Publikováno v:
ResearcherID
Benzophenone-sensitized reactions of 4-diazotetrahydrofuran-3(2H)-ones with H-donors such as tetrahydrofuran, 1,4-dioxane, cyclohexane and diethyl ether, occur without elimination of nitrogen and give rise to the corresponding N-substituted hydrazone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b34a7a8db52658d17edda9e620131b1
https://doi.org/10.1002/ajoc.201600050
https://doi.org/10.1002/ajoc.201600050
Publikováno v:
Synthesis. 47:1469-1478
Eco-friendly routes to 2,2,5,5-tetrasubstituted 4-diazodihydrofuran-3(2 H )-ones were developed. In this manner, useful precursors to oxetane derivatives, potential NSAIDs, and other biologically active pharmaceuticals can be prepared without use of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d07b0bbfa91d004cbc32f276dcce1a00
https://doi.org/10.1055/s-0034-1380268
https://doi.org/10.1055/s-0034-1380268
Publikováno v:
ChemInform. 47
Benzophenone-sensitized reactions of 4-diazotetrahydrofuran-3(2H)-ones with H-donors such as tetrahydrofuran, 1,4-dioxane, cyclohexane and diethyl ether, occur without elimination of nitrogen and give rise to the corresponding N-substituted hydrazone
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::408d1b4a6e68c4167c3aca651b59f8ee
https://doi.org/10.1002/chin.201639116
https://doi.org/10.1002/chin.201639116
Publikováno v:
Russian Journal of Organic Chemistry. 46:1542-1545
The formation of C–H insertion products in the course of direct photolysis of α,α-diphenylsubstituted diazo ketones of the tetrahydrofuran series was rationalized by secondary photochemical processes which give rise to benzophenone acting as a se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2bb61eba2ac0deb920c9979c96d1320
https://doi.org/10.1134/s1070428010100179
https://doi.org/10.1134/s1070428010100179
Publikováno v:
ChemInform. 46
The developed reaction sequence provides 2,2,5,5-tetraalkyl, 2,2,5,5-tetraaryl as well as regioisomeric 2,2-diaryl-5,5-dimethyl and 2,2-dimethyl-5,5-diaryldiazofuranones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::feb8f4345ceb099ffcccbcb9182214b0
https://doi.org/10.1002/chin.201538119
https://doi.org/10.1002/chin.201538119
Autor:
Lothar Hennig, Liudmila L. Rodina, Bärbel Schulze, Vs. V. Nikolaev, Valerij A. Nikolaev, Jochim Sieler
Publikováno v:
Russian Journal of Organic Chemistry. 40:740-746
Catalytic decomposition of diazoacetylacetone, ethyl diazoacetate, and diethyl diazomalonate effected by dirhodium tetraacetate in the presence of 3(2H)-oxoisothiazole-1,1-dioxides resulted in O-alkylation of amide carbonyl of the heterocycle affordi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0f2066935414d038b54e3022328df272
https://doi.org/10.1023/b:rujo.0000043724.25474.51
https://doi.org/10.1023/b:rujo.0000043724.25474.51