Приказ основних података о документу

endo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidines

dc.creatorStojanović, Milovan
dc.creatorMarković, Rade
dc.creatorKleinpeter, Erich
dc.creatorBaranac-Stojanović, Marija
dc.date.accessioned2019-01-30T17:26:20Z
dc.date.available2019-01-30T17:26:20Z
dc.date.issued2011
dc.identifier.issn0040-4020
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/814
dc.description.abstractendo-Mode cyclizations of vinylogous N-acyliminium ions incorporating heteroatom-based nucleophiles have been examined as a route to the synthesis of condensed thiazolidines. The scope of these reactions and stereochemical outcome are discussed and explained using quantum chemical calculations.en
dc.publisherOxford : Pergamon-Elsevier Science Ltd
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142007/RS//
dc.relationDeutscher Akademischer Austauschdienst (DAAD) [504 252 70]
dc.rightsrestrictedAccess
dc.sourceTetrahedron
dc.subjectVinylogous N-acyliminium ionen
dc.subjectendo-Mode cyclizationen
dc.subjectCondensed thiazolidinesen
dc.subjectQuantum chemical calculationsen
dc.titleendo-Mode cyclizations of vinylogous N-acyliminium ions as a route to the synthesis of condensed thiazolidinesen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractБаранац-Стојановиц, Марија; Стојановић, Милован; Клеинпетер, Ерицх; Марковиц, Раде;
dc.citation.volume67
dc.citation.issue49
dc.citation.spage9541
dc.citation.epage9554
dc.citation.other67(49): 9541-9554
dc.citation.rankM21
dc.identifier.doi10.1016/j.tet.2011.10.011
dc.identifier.scopus2-s2.0-80555122817
dc.identifier.wos000297777700012
dc.type.versionpublishedVersion


Документи

Thumbnail
Име:
812.pdf
Величина:
1.074Mb
Формат:
PDF
Отварање

Овај документ се појављује у следећим колекцијама

Приказ основних података о документу