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dc.contributor.authorPorubsky, M
dc.contributor.authorTenora, L
dc.contributor.authorPotacek, M
dc.date.accessioned2021-02-05T01:22:05Z
dc.date.available2021-02-05T01:22:05Z
dc.date.issued2016-02-01
dc.identifierpii: molecules21020187
dc.identifier.citationPorubsky, M., Tenora, L. & Potacek, M. (2016). 1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation. MOLECULES, 21 (2), https://doi.org/10.3390/molecules21020187.
dc.identifier.issn1420-3049
dc.identifier.urihttp://hdl.handle.net/11343/260370
dc.description.abstractThis paper describes the synthesis of precursors with a benzo[b]furan skeleton for the intramolecular 1,3-dipolar cycloaddition of azomethine ylides prepared from N-substituted 3-allyl-aminobenzo[b]furan-2-aldehydes and secondary amines derived from α-amino acid esters. Reactions were initiated by heating. The products consisted of four fused rings with three stereogenic centers. Their structure and stereochemistry were determined by NMR spectra and X-ray measurements.
dc.languageEnglish
dc.publisherMDPI
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.title1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation
dc.typeJournal Article
dc.identifier.doi10.3390/molecules21020187
melbourne.affiliation.departmentSchool of Chemistry
melbourne.affiliation.facultyScience
melbourne.source.titleMolecules
melbourne.source.volume21
melbourne.source.issue2
dc.rights.licenseCC BY
melbourne.elementsid1056580
dc.identifier.eissn1420-3049
melbourne.accessrightsOpen Access


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