Sökning: "Kálmán Szabó"

Visar resultat 6 - 10 av 25 avhandlingar innehållade orden Kálmán Szabó.

  1. 6. Transition Metal Mediated Transformations of Carboranes

    Författare :Ludvig Eriksson; Kalman Szabo; Uppsala universitet; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES; Chemistry; carborane; isoquinoline; PK11195; peripheral bensodiazepine receptor; Cu I Iodide; iodinated carborane; palladium; isotopic exchange; Herrmann’s Catalyst; Heck reaction; Suzuki-Miyaura reaction; cross coupling; arylation; olefination; 125-iodine; radiolabelling; carboraneboronic ester; BNCT; 2-iodo-; Kemi; Chemistry; Kemi; organisk kemi; Organic Chemistry;

    Sammanfattning : This thesis describes the use of copper and palladium to mediate transformations of carboranes, especially p-carborane.1-(1-p-carboranyl)-N-methyl-N-(2-butyl)-3-isoquinolinecarboxamide, a carborane containing analogue of the peripheral benzodiazepine receptor (PBR) ligand PK11195, has been synthesised. LÄS MER

  2. 7. Silaborations of Unsaturated Compounds

    Författare :Martin Gerdin; Christina Moberg; Kálmán Szabó; KTH; []
    Nyckelord :MEDICIN OCH HÄLSOVETENSKAP; MEDICAL AND HEALTH SCIENCES; allylboration; bismetallation; boron; carbocyclization; catalysis; 1; 3-diene; enantioselective; 1; 6-enyne; interelement; N-heterocyclic carbene; nickel; palladium; phosphine; phosphoramidite; platinum; reaction mechanism; silaboration; silicon; silylborane; stereoselective; Chemistry; Kemi;

    Sammanfattning : This thesis deals with the development of transition metal-catalyzed silaborations of 1,3-dienes and 1,6-enynes. The first part of the thesis describes the development of the enantioselective 1,4-silaboration of 1,3-cyclohexadiene. A number of chiral metal-ligand complexes were evaluated. LÄS MER

  3. 8. Novel Applications of Benziodoxole Reagents in the Synthesis of Organofluorine Compounds

    Författare :Nadia O. Ilchenko; Kálmán J. Szabó; Cristina Nevado; Stockholms universitet; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES; trifluoromethylation; hypervalent iodine; Togni reagent; difluorination; iodofluorination; organisk kemi; Organic Chemistry;

    Sammanfattning : This thesis concerns method development of new synthetic routes by applying electrophilic hypervalent iodine reagents, such as trifluoromethyl-benziodoxole (Togni reagent) and fluoro-benziodoxole. The first project involved the addition of an oxygen moiety and trifluoromethyl group across double and triple bonds (both groups derived from the hypervalent iodine reagent). LÄS MER

  4. 9. Oxidative Trifluoromethylation and other Functionalization Reactions of Alkenes and Alkynes

    Författare :Pär Janson; Kálmán Szabó; Antonio Togni; Stockholms universitet; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES; palladium; copper; transition metal; trifluoromethylation; catalysis; acetoxylation; difunctionalization; oxidation; mechanistic study; alkenes; alkynes; quinones; organisk kemi; Organic Chemistry;

    Sammanfattning : This thesis concerns the use of various potent oxidants in organic synthesis. The main focus is directed at selectively introducing trifluoromethyl groups into compounds containing double or triple bonds. All reactions proceed under mild conditions and can in most cases be performed on the bench-top. LÄS MER

  5. 10. Synthesis of Organoboronic Acids and Applications in Asymmetric Organocatalysis

    Författare :Sybrand Jonker; Kálmán Szabó; Jörg Pietruszka; Stockholms universitet; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES; Boronic acid; BINOL; allylboration; propargylation; homologation; stereoselective synthesis; asymmetric synthesis; organocatalysis; allylboronic acid; allenylboronic acid; organisk kemi; Organic Chemistry;

    Sammanfattning : Allyl- and allenylboronic acids are valuable reagents in organic synthesis due to their configurational stability and high reactivity. Few allyl- and allenylboronates are commercially available. Therefore, both the preparation and synthetic application of these organoboronic acids are subjects of study. LÄS MER