| dc.contributor.author | Porubsky, M | |
| dc.contributor.author | Tenora, L | |
| dc.contributor.author | Potacek, M | |
| dc.date.accessioned | 2021-02-05T01:22:05Z | |
| dc.date.available | 2021-02-05T01:22:05Z | |
| dc.date.issued | 2016-02-01 | |
| dc.identifier | pii: molecules21020187 | |
| dc.identifier.citation | Porubsky, 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.issn | 1420-3049 | |
| dc.identifier.uri | http://hdl.handle.net/11343/260370 | |
| dc.description.abstract | This 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.language | English | |
| dc.publisher | MDPI | |
| dc.rights.uri | https://creativecommons.org/licenses/by/4.0 | |
| dc.title | 1,3-Dipolar Cycloaddition in the Preparation of New Fused Heterocyclic Compounds via Thermal Initiation | |
| dc.type | Journal Article | |
| dc.identifier.doi | 10.3390/molecules21020187 | |
| melbourne.affiliation.department | School of Chemistry | |
| melbourne.affiliation.faculty | Science | |
| melbourne.source.title | Molecules | |
| melbourne.source.volume | 21 | |
| melbourne.source.issue | 2 | |
| dc.rights.license | CC BY | |
| melbourne.elementsid | 1056580 | |
| dc.identifier.eissn | 1420-3049 | |
| melbourne.accessrights | Open Access | |
