23 research outputs found

    PREPARATION AND X-RAY STRUCTURE OF A NEW ORGANO-P-O-S HETEROCYCLE

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    Reaction of 1,3-epithio-1 lambda(5),3 lambda(5)-naphtho[1,8-cd][1,2,6]thiadiphohosphinine-1,3-dithione 5 with 3,5-di-tert-butylcatechol gives 3,5-di-tert-butyl-1,8-epithio-1 lambda(5),8 lambda(5)-naphtho[1,8 -cd][1,7,2,6]benzodioxadiphosphonine-1,8-dithione 7 which, from X-ray studies, contains fused C3P2S and C2O2P2S rings

    PREPARATION AND X-RAY STRUCTURE OF A NEW ORGANO-P-O-S HETEROCYCLE

    No full text
    Reaction of 1,3-epithio-1 lambda(5),3 lambda(5)-naphtho[1,8-cd][1,2,6]thiadiphohosphinine-1,3-dithione 5 with 3,5-di-tert-butylcatechol gives 3,5-di-tert-butyl-1,8-epithio-1 lambda(5),8 lambda(5)-naphtho[1,8 -cd][1,7,2,6]benzodioxadiphosphonine-1,8-dithione 7 which, from X-ray studies, contains fused C3P2S and C2O2P2S rings

    cis -Dichloridobis(triisopropoxyphosphine)platinum(II)

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    cis -Dichloridobis(dimethoxyphenylphosphine)palladium(II)

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    cis -Dichloridobis(trimethoxyphosphine)palladium(II) at 125 K

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    Synthesis of bulky, electron rich hemilabile phosphines and their application in the Suzuki coupling reaction of aryl chlorides

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    Novel electron rich, amine functionalised phosphines have been prepared and shown to belong to an unusual class of ligands that can activate palladium complexes to catalyse the Suzuki coupling reaction of chloroarenes.</p
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