1. Электронный научный архив УрФУ
  2. 00. Общеуниверситетские коллекции
  3. Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC
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dc.contributor.authorVakarov, S. A.en
dc.contributor.authorChulakov, E. N.en
dc.contributor.authorSadretdinova, L. S.en
dc.contributor.authorKodess, M. I.en
dc.contributor.authorEzhikova, M. A.en
dc.contributor.authorPervova, M. G.en
dc.contributor.authorGanebnykh, I. N.en
dc.contributor.authorLevit, G. L.en
dc.contributor.authorKrasnov, V. P.en
dc.date.accessioned2021-08-31T15:04:57Z-
dc.date.available2021-08-31T15:04:57Z-
dc.date.issued2020-
dc.identifier.citationKinetic Resolution of Racemic 2-Aryloxy Propionyl Chlorides Using Enantiopure (S)-3,4-Dihydro-3-methyl-2H-[1,4]benzoxazines / S. A. Vakarov, E. N. Chulakov, L. S. Sadretdinova, et al. — DOI 10.1002/slct.202000629 // ChemistrySelect. — 2020. — Vol. 5. — Iss. 13. — P. 4069-4073.en
dc.identifier.issn23656549-
dc.identifier.otherFinal2
dc.identifier.otherAll Open Access, Bronze3
dc.identifier.otherhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85084705676&doi=10.1002%2fslct.202000629&partnerID=40&md5=d9972989bd59b54a36752ed60feeb128
dc.identifier.urihttp://elar.urfu.ru/handle/10995/102696-
dc.description.abstractStereoselectivity in the mutual kinetic resolution (KR) of racemic 3,4-dihydro-3-methyl-2H-[1,4]benzoxazines and racemic 2-aryloxy propionyl chlorides was studied. Based on the results obtained, preparative methods for single enantiomers of a series of 2-aryloxy propionic acids via acylative KR of their racemates with enantiopure (S)-3,4-dihydro-3-methyl-2H-[1,4]benzoxazines have been proposed. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheimen
dc.description.sponsorshipThe work was financially supported by the Russian Science Foundation (grant 19‐13‐00231, in the part of studying mutual kinetic resolution) and the Russian Foundation for Basic Research (grant 18‐33‐00027_mol_a, in the part of preparation of enantiomers of 2‐aryloxy propionic acids). Analytical studies were carried out using equipment of the Centre for Joint Use “Spectroscopy and Analysis of Organic Compounds” at the Postovsky Institute of Organic Synthesis, Russian Academy of Sciences (Ural Branch)en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.publisherWiley-Blackwellen
dc.relationinfo:eu-repo/grantAgreement/RSF//19-13-00231en
dc.rightsinfo:eu-repo/semantics/openAccessen
dc.sourceChemistrySelect2
dc.sourceChemistrySelecten
dc.subjectACYL CHLORIDESen
dc.subjectACYLATIONen
dc.subjectBENZOXAZINESen
dc.subjectKINETIC RESOLUTIONen
dc.subjectSTEREOSELECTIVITYen
dc.titleKinetic Resolution of Racemic 2-Aryloxy Propionyl Chlorides Using Enantiopure (S)-3,4-Dihydro-3-methyl-2H-[1,4]benzoxazinesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/articleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.identifier.doi10.1002/slct.202000629-
dc.identifier.scopus85084705676-
local.contributor.employeeVakarov, S.A., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation
local.contributor.employeeChulakov, E.N., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation
local.contributor.employeeSadretdinova, L.S., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation
local.contributor.employeeKodess, M.I., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation, Institute of Chemical Engineering, Ural Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federation
local.contributor.employeeEzhikova, M.A., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation
local.contributor.employeePervova, M.G., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation
local.contributor.employeeGanebnykh, I.N., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation
local.contributor.employeeLevit, G.L., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation
local.contributor.employeeKrasnov, V.P., Postovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation, Institute of Chemical Engineering, Ural Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federation
local.description.firstpage4069-
local.description.lastpage4073-
local.issue13-
local.volume5-
local.contributor.departmentPostovsky Institute of Organic Synthesis of RAS (Ural Branch) 22/20 S. Kovalevskoy/Akademicheskaya St., Ekaterinburg, 620108, Russian Federation
local.contributor.departmentInstitute of Chemical Engineering, Ural Federal University, 19 Mira St., Ekaterinburg, 620002, Russian Federation
local.identifier.pure12670812-
local.identifier.eid2-s2.0-85084705676-
local.fund.rsf19-13-00231-
local.fund.rffi18-33-00027-
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