Synthesis and Characterization of 6-Bromo-Benzoflavanone Derivatives
| dc.contributor.advisor | Kónya, Krisztina | |
| dc.contributor.author | Amin, Yasmin | |
| dc.contributor.department | DE--Természettudományi és Technológiai Kar--Kémiai Intézet | |
| dc.date.accessioned | 2024-12-18T07:33:50Z | |
| dc.date.available | 2024-12-18T07:33:50Z | |
| dc.date.created | 2024-11-14 | |
| dc.description.abstract | This thesis presents the development of an efficient synthesis pathway for 6-bromo-benzoflavanone as aromatase inhibition for cancer treatment, aiming to optimize yield and enhance stereoselectivity. The process begins with the bromination of 1-(1-hydroxynaphthalen-2-yl)ethan-1-one, followed by protection of the hydroxyl group, and Claisen-Schmidt condensation to form chalcone derivatives with variable yields. Microwave-assisted cyclization using trifluoroacetic acid was employed after unsuccessful attempts with other cyclization methods, resulting in a 28% yield of the target flavanone compound. Then the 6-bromo-benzoflavanone is utilized as a reference compound in rhodium-catalyzed asymmetric 1,4-addition of arylboronic acids to chromenones, yielding high enantioselectivities, and its structure was confirmed through NMR. | |
| dc.description.course | Biochemical engineering | |
| dc.description.degree | BSc/BA | |
| dc.format.extent | 29 | |
| dc.identifier.uri | https://hdl.handle.net/2437/383832 | |
| dc.language.iso | en | |
| dc.rights.access | Hozzáférhető a 2022 decemberi felsőoktatási törvénymódosítás értelmében. | |
| dc.subject | Flavonoids | |
| dc.subject | Microwave-Assisted Synthesis | |
| dc.subject | Enantioselective Synthesis | |
| dc.subject | Claisen-Schmidt condensation | |
| dc.subject | Cyclization | |
| dc.subject | Aromatase Inhibition | |
| dc.subject.dspace | Chemistry | |
| dc.title | Synthesis and Characterization of 6-Bromo-Benzoflavanone Derivatives |
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