| dc.contributor.author | Zissimou, Georgia A. | en |
| dc.contributor.author | Kourtellaris, Andreas | en |
| dc.contributor.author | Koutentis, Panayiotis A. | en |
| dc.creator | Zissimou, Georgia A. | en |
| dc.creator | Kourtellaris, Andreas | en |
| dc.creator | Koutentis, Panayiotis A. | en |
| dc.date.accessioned | 2021-01-25T09:44:46Z | |
| dc.date.available | 2021-01-25T09:44:46Z | |
| dc.date.issued | 2018 | |
| dc.identifier.issn | 0022-3263 | |
| dc.identifier.uri | http://gnosis.library.ucy.ac.cy/handle/7/63018 | |
| dc.description.abstract | Isodiphenylfluorindone 6 and isodiphenylfluorindinone 7 are synthesized. The former reacts with NaOMe to give the 13-methoxyisodiphenylfluorindone 22 (95%), while the latter reacts with 70% perchloric acid to give the bisperchlorate 21 (87%) and with MnO2 dimerizes to give 13,13′-bi(isodiphenylfluorindone) 4 (60%). UV–vis, NMR, CV, and DFT computational studies support the structural assignments of all products. Single-crystal X-ray diffraction studies are reported for isodiphenylfluorindinone 7. | en |
| dc.source | The Journal of Organic Chemistry | en |
| dc.source.uri | https://doi.org/10.1021/acs.joc.8b00554 | |
| dc.title | Synthesis and Characterization of Isodiphenylfluorindone and Isodiphenylfluorindinone | en |
| dc.type | info:eu-repo/semantics/article | |
| dc.identifier.doi | 10.1021/acs.joc.8b00554 | |
| dc.description.volume | 83 | |
| dc.description.issue | 8 | |
| dc.description.startingpage | 4754 | |
| dc.description.endingpage | 4761 | |
| dc.author.faculty | 002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences | |
| dc.author.department | Τμήμα Χημείας / Department of Chemistry | |
| dc.type.uhtype | Article | en |
| dc.source.abbreviation | J. Org. Chem. | en |
| dc.contributor.orcid | Zissimou, Georgia A. [0000-0003-4821-9469] | |
| dc.contributor.orcid | Koutentis, Panayiotis A. [0000-0002-4652-7567] | |
| dc.gnosis.orcid | 0000-0003-4821-9469 | |
| dc.gnosis.orcid | 0000-0002-4652-7567 | |
