1. Synthesis of naphthalene-based push-pull molecules with a heteroaromatic electron acceptorDavid Šarlah, Amadej Juranovič, Boris Kožar, Luka Rejc, Amalija Golobič, Andrej Petrič, 2016, original scientific article Keywords: FDDNP analogs, push-pull dyes, heterocyclization, cross-coupling reactions, UV/vis spectroscopy Full text (file, 1,61 MB) This document has more files! More... |
2. Microwave-assisted regioselective Suzuki coupling of 2,4-dichloropyrimidines with aryl and heteroaryl boronic acidsAna Dolšak, Kristjan Mrgole, Matej Sova, 2021, original scientific article Keywords: cross-coupling, Suzuki, palladium, pyrimidines, synthesis, microwave-assisted Full text (file, 1,75 MB) This document has more files! More... |
3. Catalytic photoredox C–H arylation of 4-oxo-4H-pyrido[1,2-a]pyrimidine-3-diazonium tetrafluoroborates and related heteroaryl diazonium saltsKris Antolinc, Helena Brodnik Žugelj, Uroš Grošelj, Bogdan Štefane, Nejc Petek, Jurij Svete, 2023, original scientific article Keywords: quinolizines, pyrido[1, 2-a]pyrimidines, thiazolo[3, 2-a]pyrimidines, photoredox catalysis, arylation, cross-coupling, chemical reactions, mixtures, molecular structure, salts Full text (file, 1,93 MB) This document has more files! More... |
4. Carbonyl-supported coordination in imidazolatesAljaž Škrjanc, Dominik Jankovič, Anton Meden, Matjaž Mazaj, Erik Svensson Grape, Martin Gazvoda, Nataša Zabukovec Logar, 2024, original scientific article Keywords: heterogeneous catalysis, nickel catalysis, Suzuki–Miyaura cross coupling, zeolitic imidazolate frameworks Full text (file, 1,50 MB) This document has more files! More... |
5. The versatile and strategic O-carbamate directed metalation group in the synthesis of aromatic moleculesRoss D. Jansen-van Vuuren, Susana Liu, M. A. Jalil Miah, Janez Cerkovnik, Janez Košmrlj, Victor Snieckus, 2024, review article Keywords: aryl O-carbamate, metalation, rearrangement, cross coupling, regioselective, directing group, aromatic compounds, hydrocarbons, organic compounds Full text (file, 14,53 MB) This document has more files! More... |