Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis

Simple item page
dc.contributor.authorAlbota, Florin
dc.contributor.authorCaira, Mino R
dc.contributor.authorDraghici, Constantin
dc.contributor.authorDumitrascu, Florea
dc.contributor.authorDumitrescu, Denisa E
dc.date.accessioned2021-10-08T06:20:13Z
dc.date.available2021-10-08T06:20:13Z
dc.date.issued2016
dc.description.abstractThe synthesis of sydnones heteroarylated at C-4 with an indolizine was achieved by Chichibabin (Tschitschibabin) indolizine synthesis starting from the corresponding sydnone-N-pyridinium bromides. The latter compounds were also transformed to sydnone-indolizines connected through a keto group at the C-4 position by refluxing them in 1,2-epoxybutane with an activated alkyne. The structures of the new compounds were assigned by FTIR, NMR spectroscopy and X-ray analysis.
dc.identifier.apacitationAlbota, F., Caira, M. R., Draghici, C., Dumitrascu, F., & Dumitrescu, D. E. (2016). Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis. <i>Beilstein Journal of Organic Chemistry</i>, 12(4), 2503 - 2510. http://hdl.handle.net/11427/34225en_ZA
dc.identifier.chicagocitationAlbota, Florin, Mino R Caira, Constantin Draghici, Florea Dumitrascu, and Denisa E Dumitrescu "Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis." <i>Beilstein Journal of Organic Chemistry</i> 12, 4. (2016): 2503 - 2510. http://hdl.handle.net/11427/34225en_ZA
dc.identifier.citationAlbota, F., Caira, M.R., Draghici, C., Dumitrascu, F. & Dumitrescu, D.E. 2016. Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis. <i>Beilstein Journal of Organic Chemistry.</i> 12(4):2503 - 2510. http://hdl.handle.net/11427/34225en_ZA
dc.identifier.issn1860-5397
dc.identifier.issn2195-951X
dc.identifier.ris TY - Journal Article AU - Albota, Florin AU - Caira, Mino R AU - Draghici, Constantin AU - Dumitrascu, Florea AU - Dumitrescu, Denisa E AB - The synthesis of sydnones heteroarylated at C-4 with an indolizine was achieved by Chichibabin (Tschitschibabin) indolizine synthesis starting from the corresponding sydnone-N-pyridinium bromides. The latter compounds were also transformed to sydnone-indolizines connected through a keto group at the C-4 position by refluxing them in 1,2-epoxybutane with an activated alkyne. The structures of the new compounds were assigned by FTIR, NMR spectroscopy and X-ray analysis. DA - 2016 DB - OpenUCT DP - University of Cape Town IS - 4 J1 - Beilstein Journal of Organic Chemistry LK - https://open.uct.ac.za PY - 2016 SM - 1860-5397 SM - 2195-951X T1 - Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis TI - Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis UR - http://hdl.handle.net/11427/34225 ER - en_ZA
dc.identifier.urihttp://hdl.handle.net/11427/34225
dc.identifier.vancouvercitationAlbota F, Caira MR, Draghici C, Dumitrascu F, Dumitrescu DE. Sydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis. Beilstein Journal of Organic Chemistry. 2016;12(4):2503 - 2510. http://hdl.handle.net/11427/34225.en_ZA
dc.language.isoeng
dc.publisher.departmentDepartment of Chemistry
dc.publisher.facultyFaculty of Science
dc.sourceBeilstein Journal of Organic Chemistry
dc.source.journalissue4
dc.source.journalvolume12
dc.source.pagination2503 - 2510
dc.source.urihttps://dx.doi.org/10.3762/bjoc.12.245
dc.subject.otherbiheteroaryl
dc.subject.otherChichibabin synthesis
dc.subject.otherindolizine
dc.subject.otherpyridinium N-ylide
dc.subject.othersydnone
dc.titleSydnone C-4 heteroarylation with an indolizine ring via Chichibabin indolizine synthesis
dc.typeJournal Article
uct.type.publicationResearch
uct.type.resourceJournal Article
Files
Original bundle
Now showing 1 - 1 of 1
Thumbnail Image
Name:
AlbotaFlorin_Sydnone_C_4_het_2016.pdf
Size:
978.62 KB
Format:
Adobe Portable Document Format
Description:
Download
Collections
Journal Articles