izpis_h1_title_alt

Rutenij/paladij dvojno ariliranje 3-heteroarilizokinolinov
ID Pečarič Strnad, Tina (Author), ID Štefane, Bogdan (Mentor) More about this mentor... This link opens in a new window

.pdfPDF - Presentation file, Download (2,24 MB)
MD5: 8E6B8D455620A164BEAD4831E52E2970

Abstract
V magistrski nalogi smo izvajali rutenij katalizirano neposredno C–H ariliranje 3-heteroarilizokinolinov, kateremu je sledilo paladij katalizirano neposredno C–H ariliranje. Uspešno smo optimizirali reakcijske pogoje obeh stopenj tako, da smo dosegli optimalno stopnjo pretvorbe. Z uporabo optimiziranih pogojev smo sintetizirali več različnih monoariliranih in nekaj diariliranih produktov. Nadalje smo optimizirane reakcijske pogoje uporabili pri izvedbi sekvenčne »one-pot« reakcije za sintezo končnih diariliranih produktov, saj nas je zanimalo ali je sekvenčna »one-pot« metoda enako učinkovita, kot če reakcijo izvedemo stopenjsko s čiščenjem vmesnega intermediata. S primerjavo izkoristkov končnih produktov smo ugotovili, da sta oba načina sinteze diariliranih produktov podobno učinkovita.

Language:Slovenian
Keywords:C–H aktivacija, 3-heteroarilizokinolin, »one-pot«, ariliranje, kataliza s kovinami prehoda
Work type:Master's thesis/paper
Typology:2.09 - Master's Thesis
Organization:FKKT - Faculty of Chemistry and Chemical Technology
Year:2020
PID:20.500.12556/RUL-117091 This link opens in a new window
COBISS.SI-ID:20941827 This link opens in a new window
Publication date in RUL:23.06.2020
Views:2542
Downloads:269
Metadata:XML DC-XML DC-RDF
:
Copy citation
Share:Bookmark and Share

Secondary language

Language:English
Title:Ruthenium/palladium diarylation of 3-heteroarylisoquinolines
Abstract:
The master thesis describes ruthenium catalyzed direct C–H arylation of 3-heteroarylisoquinolines, followed by palladium catalyzed direct C–H arylation. We successfully optimized the reaction conditions of both steps to achieve the optimum conversion. Several different monoarylated and some diarylated products were synthesized using the optimized conditions. We further used the optimized conditions to perform a sequential one-pot reaction for the synthesis of the final diarylated products. We were interested in whether the sequential one-pot method was as effective as if the reactions was performed sequentially with purification of the intermediate. By comparing the yields of the products, we concluded that both modes of synthesis of diarylated products are similarly effective.

Keywords:C–H activation, 3-heteroarylisoquinoline, one-pot, arylation, transition-metal catalysis

Similar documents

Similar works from RUL:
Similar works from other Slovenian collections:

Back