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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/19508
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dc.contributor.authorAksenov, N. A.-
dc.contributor.authorАксенов, Н. А.-
dc.contributor.authorAksenov, A. V.-
dc.contributor.authorАксенов, А. В.-
dc.contributor.authorPrityko, L. A.-
dc.contributor.authorПритыко, Л. А.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorAksenova, D. S.-
dc.contributor.authorАксенова, Д. С.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2022-05-05T12:54:16Z-
dc.date.available2022-05-05T12:54:16Z-
dc.date.issued2022-
dc.identifier.citationAksenov, N. A., Aksenov, A. V., Prityko, L. A., Aksenov, D. A., Aksenova, D. S., Nobi, M. A., Rubin, M. Oxidative Cyclization of 4-(2-Aminophenyl)-4-oxo-2-phenylbutanenitriles into 2-(3-Oxoindolin-2-ylidene)acetonitriles // ACS Omega. - 2022. - DOI10.1021/acsomega.2c01238ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/19508-
dc.description.abstractA facile and highly efficient method for the preparation of 2-(3-oxoindolin-2-ylidene)acetonitriles from 4-(2-aminophenyl)-4-oxo-2-phenylbutanenitriles is described. The featured transformation operates via nucleophilic intramolecular cyclization and involves oxidation of the aniline moiety. Overall, this modification allowed for the improvement of yields and expansion of the reaction scope.ru
dc.language.isoenru
dc.publisherAmerican Chemical Societyru
dc.relation.ispartofseriesACS Omega-
dc.subjectOxidative cyclizationru
dc.subjectOxidation of the aniline moietyru
dc.subjectNucleophilic intramolecular cyclizationru
dc.titleOxidative Cyclization of 4-(2-Aminophenyl)-4-oxo-2-phenylbutanenitriles into 2-(3-Oxoindolin-2-ylidene)acetonitrilesru
dc.typeСтатьяru
vkr.instХимико-фармацевтический факультетru
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