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  1. 1. New Applications of Monoorganocopper/Iodotrimethylsilane Reagents in Conjugate Additions

    Författare :Magnus Eriksson; Chalmers tekniska högskola; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES; beta-unsaturated; halosilane; conjugate addition; alpha; copper iodide; copper acetylides; organocopper; iodotrimethylsilane; Claisen rearrangement;

    Sammanfattning : The thesis reports new applications of monoorganocopper compounds, RCu(LiI), and iodotrimethylsilane in conjugate additions. The present investigation demonstrates conjugate addition of alkylcopper compounds and iodotrimethylsilane to reactive .alpha.,. LÄS MER

  2. 2. Synthesis and [3,3]-Sigmatropic Rearrangement of Vinylaziridines

    Författare :Ulf Lindström; Torbjörn Frejd; Stockholms universitet; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES; Organic chemistry; Organisk kemi; Organic Chemistry; organisk kemi;

    Sammanfattning : A general synthetic route from vinylepoxides to vinylaziridines via 1,2-amino alcohols was developed. The 1,2-amino alcohols were obtained from a stereospecific and regioselective aminolysis of vinylepoxides. The synthetic scope of the aminolysis could be expanded by the use of a microwave-assisted protocol. LÄS MER

  3. 3. Synthesis Towards Biologically Active Natural Products

    Författare :Rikard Larsson; Centrum för analys och syntes; []
    Nyckelord :NATURVETENSKAP; NATURAL SCIENCES; Transtaganolide; basiliolide; natural product; total synthesis; biomimetic; Thapsia; Diels-Alder; Ireland-Claisen; Pictet-Spengler; tetrahydroisoquinoline; indole;

    Sammanfattning : In 2005 two research groups independently reported the isolation of a series of structurally intriguing C-19 terpenolides from the plants Thapsia transtagana and Thapsia garganica. The compounds were shown to be potent inhibitors of the sarco/endoplasmic reticulum Ca2+-ATPases. LÄS MER