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dc.contributor.authorKorotaev, V. Y.en
dc.contributor.authorBarkov, A. Y.en
dc.contributor.authorMoshkin, V. S.en
dc.contributor.authorMatochkina, E. G.en
dc.contributor.authorKodess, M. I.en
dc.contributor.authorSosnovskikh, V. Y.en
dc.date.accessioned2014-11-29T19:45:52Z-
dc.date.available2014-11-29T19:45:52Z-
dc.date.issued2013-
dc.identifier.citationHighly diastereoselective 1,3-dipolar cycloaddition of nonstabilized azomethine ylides to 3-nitro-2-trihalomethyl-2H-chromenes: Synthesis of 1-benzopyrano[3,4-c]pyrrolidines / V. Y. Korotaev, A. Y. Barkov, V. S. Moshkin [et al.] // Tetrahedron. — 2013. — Vol. 69. — № 40. — P. 8602-8608.en
dc.identifier.issn0040-4020-
dc.identifier.other1good_DOI
dc.identifier.otherfa8a9eda-4449-48ff-86be-564d74b005b0pure_uuid
dc.identifier.otherhttp://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=84882875236m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/27144-
dc.description.abstractReactions of 3-nitro-2-trifluoro(trichloro)methyl-2H-chromenes, including 2-unsubstituted derivatives, with N-alkyl-α-amino acids (sarcosine, proline) and paraformaldehyde proceed diastereoselectively to give 1-benzopyrano[3,4-c]pyrrolidines in good yields as a result of a 1,3-dipolar cycloaddition of the intermediate nonstabilized azomethine ylide at the Δ3-bond of the chromene system. © 2013 Elsevier Ltd. All rights reserved.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.sourceTetrahedronen
dc.subject1,3-DIPOLAR CYCLOADDITIONen
dc.subject1-BENZOPYRANO[3,4-C]PYRROLIDINESen
dc.subject3-NITRO-2H-CHROMENESen
dc.subjectNONSTABILIZED AZOMETHINE YLIDESen
dc.subject2 BROMO 6A NITRO 6 (TRICHLOROMETHYL) 6,6A,6B,7,8,9,11,11A OCTAHYDROCHROMENO[3,4 A]PYRROLIZINEen
dc.subject2 BROMO 6A NITRO 6 (TRIFLUOROMETHYL) 6,6A,6B,7,8,9,11,11A OCTAHYDROCHROMENO[3,4 A]PYRROLIZINEen
dc.subject2 METHYL 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE 3A CARBONITRILEen
dc.subject2 METHYL 3A NITRO 4 (TRICHLOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLEen
dc.subject2 METHYL 3A NITRO 4 (TRICHLOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE OXALATEen
dc.subject2 METHYL 3A NITRO 4 (TRIFLUOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLEen
dc.subject2 METHYL 3A NITRO 4 (TRIFLUOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE OXALATEen
dc.subject2 METHYL 3A,8 DINITRO 4 (TRICHLOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLEen
dc.subject2 METHYL 3A,8 DINITRO 4 (TRICHLOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE OXALATEen
dc.subject2 METHYL 3A,8 DINITRO 4 (TRIFLUOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLEen
dc.subject2 METHYL 3A,8 DINITRO 4 (TRIFLUOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE OXALATEen
dc.subject2 METHYL 8 METHOXY 3A NITRO 4 (TRICHLOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLEen
dc.subject2 METHYL 8 METHOXY 3A NITRO 4 (TRICHLOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE OXALATEen
dc.subject2 METHYL 8 METHOXY 3A NITRO 4 (TRIFLUOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLEen
dc.subject2 METHYL 8 METHOXY 3A NITRO 4 (TRIFLUOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE OXALATEen
dc.subject6A NITRO 6 (TRIFLUOROMETHYL) 6,6A,6B,7,8,9,11,11A OCTAHYDROCHROMENO[3,4 A]PYRROLIZINEen
dc.subject6A NITRO 6 PHENYL 6,6A,6B,7,8,9,11,11A OCTAHYDROCHROMENO[3,4 A]PYRROLIZINEen
dc.subject8 BROMO 2 METHYL 3A NITRO 4 (TRICHLOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLEen
dc.subject8 BROMO 2 METHYL 3A NITRO 4 (TRICHLOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE OXALATEen
dc.subject8 BROMO 2 METHYL 3A NITRO 4 (TRIFLUOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLEen
dc.subject8 BROMO 2 METHYL 3A NITRO 4 (TRIFLUOROMETHYL) 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE OXALATEen
dc.subjectAZOMETHINE YLIDEen
dc.subjectCHROMENE DERIVATIVEen
dc.subjectMETHYL 2 METHYL 1,2,3,3A,4,9B HEXAHYDROCHROMENO[3,4 C]PYRROLE 3A CARBOXYLATEen
dc.subjectPARAFORMALDEHYDEen
dc.subjectPYRROLIDINE DERIVATIVEen
dc.subjectUNCLASSIFIED DRUGen
dc.subjectARTICLEen
dc.subjectCONTROLLED STUDYen
dc.subjectCYCLOADDITIONen
dc.subjectDRUG SYNTHESISen
dc.subjectPRIORITY JOURNALen
dc.subjectSTEREOCHEMISTRYen
dc.subjectTRIFLUOROen
dc.titleHighly diastereoselective 1,3-dipolar cycloaddition of nonstabilized azomethine ylides to 3-nitro-2-trihalomethyl-2H-chromenes: Synthesis of 1-benzopyrano[3,4-c]pyrrolidinesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.typeinfo:eu-repo/semantics/articleen
dc.identifier.doi10.1016/j.tet.2013.07.080-
dc.identifier.scopus84882875236-
local.affiliationDepartment of Chemistry, Ural Federal University, 620000 Ekaterinburgc, Russian Federationen
local.affiliationInstitute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, 620041 Ekaterinburg, Russian Federationen
local.contributor.employeeКоротаев Владислав Юрьевичru
local.contributor.employeeБарков Алексей Юрьевичru
local.contributor.employeeМошкин Владимир Сергеевичru
local.contributor.employeeКодесс Михаил Исааковичru
local.contributor.employeeСосновских Вячеслав Яковлевичru
local.description.firstpage8602-
local.description.lastpage8608-
local.issue40-
local.volume69-
dc.identifier.wos000323873100009-
local.contributor.departmentИнститут естественных наук и математикиru
local.identifier.pure858947-
local.identifier.eid2-s2.0-84882875236-
local.identifier.wosWOS:000323873100009-
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