M
Marijan Kočevar
Researcher at University of Ljubljana
Publications - 198
Citations - 2066
Marijan Kočevar is an academic researcher from University of Ljubljana. The author has contributed to research in topics: Pyran & Catalysis. The author has an hindex of 23, co-authored 198 publications receiving 1942 citations.
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A new modification of anti-tubercular active molecules.
Aleš Imramovský,Slovenko Polanc,Jarmila Vinšová,Marijan Kočevar,Josef Jampilek,Zuzana Reckova,Jarmila Kaustová +6 more
TL;DR: The synthesis is based on derivatives that originate from isonicotinoyl hydrazide, pyrazinamide, p-aminosalicylic acid, ethambutol, and ciprofloxacin and the lipophilicity, hydrolysis, and antituberculotic activity as well as the structure-lipophILicity and structure-activity relationships are discussed.
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Preparation of rhodium nanoparticles in carbon dioxide induced ionic liquids and their application to selective hydrogenation.
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A mesoionic bis(Py-tzNHC) palladium(II) complex catalyses “green” Sonogashira reaction through an unprecedented mechanism
Martin Gazvoda,Miha Virant,Andrej Pevec,Damijana Urankar,Aljoša Bolje,Marijan Kočevar,Janez Košmrlj +6 more
TL;DR: A novel bis(pyridyl-functionalized 1,2,3-triazol-5-ylidene)-palladium(II) complex catalyses the copper-, amine-, phosphine-, and additive-free aerobic Sonogashira alkynylation of (hetero)aryl bromides in water as the only reaction solvent.
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New fluorine-containing hydrazones active against MDR-tuberculosis.
Eva Vavříková,Slovenko Polanc,Marijan Kočevar,Kata Horváti,Szilvia Bősze,Jiřina Stolaříková,Kateřina Vávrová,Jarmila Vinšová +7 more
TL;DR: Several new fluorine-containing hydrazones were synthesized and screened for their in vitro antimycobacterial activity and all evaluated compounds were found to be non-cytotoxic.
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Catalyst-free reactions under solvent-free conditions: microwave-assisted synthesis of heterocyclic hydrazones below the melting points of neat reactants.
TL;DR: The reaction of neat 5- or 8-oxobenzopyran-2(1H)-ones with a variety of aromatic and heteroaromatic hydrazines is remarkably accelerated upon irradiation in a household microwave oven in the absence of any catalyst, solid support or solvent thus providing an environmentally friendly route to several heterocyclic hydrazones.