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Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/27082
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dc.contributor.authorMoshkin, V. S.en
dc.contributor.authorSosnovskikh, V. Y.en
dc.date.accessioned2014-11-29T19:45:37Z-
dc.date.available2014-11-29T19:45:37Z-
dc.date.issued2013-
dc.identifier.citationMoshkin V. S. A one-pot synthesis of tetrahydroisoquinolin-4-ols via a novel acid-catalyzed rearrangement of 5-aryloxazolidines / V. S. Moshkin, V. Y. Sosnovskikh // Tetrahedron Letters. — 2013. — Vol. 54. — № 20. — P. 2455-2457.en
dc.identifier.issn0040-4039-
dc.identifier.other1good_DOI
dc.identifier.otherf0acc5b9-ea17-4101-8b27-a7e550dcf52fpure_uuid
dc.identifier.otherhttp://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=84876137658m
dc.identifier.urihttp://elar.urfu.ru/handle/10995/27082-
dc.description.abstractBenzaldehydes with electron-donating substituents react smoothly with a nonstabilized azomethine ylide derived from sarcosine and formaldehyde to form 5-aryloxazolidines as intermediates, which undergo rearrangement into 2-methyl-1,2,3,4-tetrahydroisoquinolin-4-ols in high yields by simple heating with hydrochloric acid. This one-pot synthesis of tetrahydroisoquinolines can be considered as a formal [3+3] cycloaddition of the azomethine ylide to the aromatic aldehyde. © 2013 Elsevier Ltd. All rights reserved.en
dc.format.mimetypeapplication/pdfen
dc.language.isoenen
dc.sourceTetrahedron Lettersen
dc.subject1,2,3,4-TETRAHYDROISOQUINOLIN-4-OLSen
dc.subject5-ARYLOXAZOLIDINESen
dc.subject[3+2] CYCLOADDITIONen
dc.subjectNONSTABILIZED AZOMETHINE YLIDEen
dc.subjectPICTET-SPENGLER REACTIONen
dc.subjectREARRANGEMENTen
dc.subject2 METHYL 1,2,3,4 TETRAHYDROISOQUINOLIN 4 OL DERIVATIVEen
dc.subject5 ARYLOXAZOLIDINE DERIVATIVEen
dc.subjectALDEHYDEen
dc.subjectFORMALDEHYDEen
dc.subjectHYDROCHLORIC ACIDen
dc.subjectOXAZOLIDINE DERIVATIVEen
dc.subjectSARCOSINEen
dc.subjectTETRAHYDROISOQUINOLINE DERIVATIVEen
dc.subjectUNCLASSIFIED DRUGen
dc.subjectARTICLEen
dc.subjectCYCLOADDITIONen
dc.subjectONE POT SYNTHESISen
dc.titleA one-pot synthesis of tetrahydroisoquinolin-4-ols via a novel acid-catalyzed rearrangement of 5-aryloxazolidinesen
dc.typeArticleen
dc.typeinfo:eu-repo/semantics/publishedVersionen
dc.typeinfo:eu-repo/semantics/articleen
dc.identifier.doi10.1016/j.tetlet.2013.02.087-
dc.identifier.scopus84876137658-
local.affiliationDepartment of Chemistry, Ural Federal University, Pr. Lenina 51, 620000 Ekaterinburg, Russian Federationen
local.contributor.employeeМошкин Владимир Сергеевичru
local.contributor.employeeСосновских Вячеслав Яковлевичru
local.description.firstpage2455-
local.description.lastpage2457-
local.issue20-
local.volume54-
dc.identifier.wos000317809900003-
local.contributor.departmentИнститут естественных наук и математикиru
local.identifier.pure910068-
local.identifier.eid2-s2.0-84876137658-
local.identifier.wosWOS:000317809900003-
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