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Allylation and heterocycloaddition reactions of aldimines: Furan- and quinolinecarboxaldehydes

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dc.contributor.authorKouznetsov, V
dc.contributor.authorOcal, N
dc.contributor.authorTurgut, Z
dc.contributor.authorZubkov, F
dc.contributor.authorKaban, S
dc.contributor.authorVarlamov, AV
dc.date.accessioned2026-06-27T12:59:46Z
dc.date.issued1998
dc.description.abstractNew derivatives of alpha-substituted furans were prepared in high yields from easily available alpha-furfurylidenbenzilamines via nucleophilic C-allylation. The homoallylamines obtained this way were used for the synthesis of some polyfunctional aminobutene derivatives. In addition, 4-thiazolidinones some of which are hetaryl substituted at the 2-position were prepared by the reaction of mercapto acids with quinoline carboxaldehydes and p-phenetidine. All new products were fully characterized.en
dc.description.urihttps://doi.org/10.1007/s007060050087
dc.identifier.doi10.1007/s007060050087
dc.identifier.endpage677
dc.identifier.issn0026-9247
dc.identifier.issue6-7
dc.identifier.startpage671
dc.identifier.urihttps://hdl.handle.net/20.500.14981/48730
dc.identifier.volume129
dc.identifier.wos000074834400013
dc.language.isoeng
dc.publisherSPRINGER-VERLAG WIEN
dc.relation.ispartofMONATSHEFTE FUR CHEMIE
dc.rightsopenAccess
dc.subjectDiels-Alder adduct
dc.subjectalpha-furfurylidenbenzilamine
dc.subjectnitrone
dc.subjectalpha-substituted furan
dc.subject4-thiazolidinone
dc.subjectChemistry
dc.titleAllylation and heterocycloaddition reactions of aldimines: Furan- and quinolinecarboxaldehydes
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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