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Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/3700
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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.authorNadein, O. N.-
dc.contributor.authorНадеин, О. Н.-
dc.contributor.authorAksenov, D. A.-
dc.contributor.authorАксенов, Д. А.-
dc.contributor.authorSmirnov, A. N.-
dc.contributor.authorСмирнов, А. Н.-
dc.contributor.authorRubin, M. A.-
dc.contributor.authorРубин, М. А.-
dc.date.accessioned2018-12-17T14:49:41Z-
dc.date.available2018-12-17T14:49:41Z-
dc.date.issued2015-
dc.identifier.citationAksenov, N.A., Aksenov, A.V., Nadein, O.N., Aksenov, D.A., Smirnov, A.N., Rubin, M. One-pot synthesis of benzoxazoles via the metal-free ortho-C-H functionalization of phenols with nitroalkanes // RSC Advances. - 2015. - Volume 5. - Issue 88. - Pages 71620-71626ru
dc.identifier.urihttp://hdl.handle.net/20.500.12258/3700-
dc.description.abstractPPA-activated nitroalkanes are employed in the design of a one-pot cascade transformation involving metal-free and oxidant-free direct ortho-C-H functionalization, followed by Beckman rearrangement and intramolecular cyclocondensation to produce benzoxazoles and benzobisoxazoles directly from easily available phenolsru
dc.language.isoenru
dc.publisherRoyal Society of Chemistryru
dc.relation.ispartofseriesRSC Advances-
dc.subjectParaffinsru
dc.subjectBenzoxazoleru
dc.subjectC-H functionalizationru
dc.subjectCascade transformationsru
dc.subjectCyclocondensationru
dc.subjectMetal freeru
dc.subjectNitroalkanesru
dc.subjectOne potru
dc.subjectOne-pot synthesisru
dc.subjectPhenolsru
dc.titleOne-pot synthesis of benzoxazoles via the metal-free ortho-C-H functionalization of phenols with nitroalkanesru
dc.typeСтатьяru
vkr.amountPages 71620-71626ru
vkr.instИнститут математики и естественных наук-
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