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dc.creatorStojanović, Milovan
dc.creatorMarković, Rade
dc.creatorKleinpeter, Erich
dc.creatorBaranac-Stojanović, Marija
dc.date.accessioned2019-11-12T11:57:29Z
dc.date.available2019-11-12T11:57:29Z
dc.date.issued2011
dc.identifier.issn0040-4020
dc.identifier.urihttps://cherry.chem.bg.ac.rs/handle/123456789/3644
dc.publisherPergamon-Elsevier Science Ltd, Oxford
dc.relationinfo:eu-repo/grantAgreement/MESTD/MPN2006-2010/142007/RS//
dc.relationDeutscher Akademischer Austauschdienst (DAAD) [504 252 70]
dc.rightsopenAccess
dc.rights.urihttps://creativecommons.org/licenses/by-sa/4.0/
dc.sourceTetrahedron
dc.subjectVinylogous N-acyliminium ionen
dc.subjectendo-Mode cyclizationen
dc.subjectCondensed thiazolidinesen
dc.subjectQuantum chemical calculationsen
dc.titleSupplementary data for article: Stojanović, M.; Marković, R.; Kleinpeter, E.; Baranac-Stojanović, M. Endo-Mode Cyclizations of Vinylogous N-Acyliminium Ions as a Route to the Synthesis of Condensed Thiazolidines. Tetrahedron 2011, 67 (49), 9541–9554. https://doi.org/10.1016/j.tet.2011.10.011en
dc.typedataset
dc.rights.licenseBY-SA
dcterms.abstractКлеинпетер, Ерицх; Марковић, Раде; Баранац-Стојановић, Марија; Стојановић, Милован;
dc.description.otherSupplementary material for: [https://doi.org/10.1016/j.tet.2011.10.011]
dc.description.otherRelated to published version: [http://cherry.chem.bg.ac.rs/handle/123456789/1226]
dc.type.versionpublishedVersionen
dc.identifier.fulltexthttps://cherry.chem.bg.ac.rs/bitstream/id/16008/endo_Mode_cyclizations_sup_2011.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_cherry_3644


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