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Showing 1 to 5 of 5 for “"1,2-Dioxolane"”.

  1. Synthesis and Chemiluminescent Investigation of Malonyl Peroxides

    The three malonyl peroxides 4-methyl-4-phenyl-1,2-dioxolane-3,5-dione (3), 4-diphenylmethyl-4-methyl-1,2-dioxolane-3,5-dione (4), and 4-methyl-4-(1-propenyl)-1,2-dioxolane-3,5-dione (5) are prepared by the methanesulfonic acid catalyzed reaction of hydrogen peroxide with the parent malonic acids. …

    uiuc Repository record for Synthesis and Chemiluminescent Investigation of Malonyl Peroxides (opens in a new tab)

  2. Preparation and Chemiluminescence of Cyclopropyl-Substituted Malonyl Peroxides

    4-Spiro{(2'-spirocyclopropyl)-cyclohexyl}-1,2-dioxolane-3,5-dione (2) and 4-cyclopropyl-4-methyl-1,2-dioxolane-3,5-dione (1) are prepared by the reaction of dicyclohexylcarbodiimide and hydrogen peroxide with the parent malonic acids. Chemiluminescence is observed when the cyclopropyl-substituted …

    uiuc Repository record for Preparation and Chemiluminescence of Cyclopropyl-Substituted Malonyl Peroxides (opens in a new tab)

  3. Synthesis of novel cycloperoxides

    … a novel synthetic route to 3,5-substituted 1,2-dioxolane ethyl esters through the chemoselective reduction of a δ-peroxy-β-keto ester to the corresponding δ-peroxy-β-hydroxy ester, and subsequent phosphorus pentoxide-mediated cyclisation. Chapter 5 outlines our preparation of several novel …

    cork Repository record for Synthesis of novel cycloperoxides (opens in a new tab)

  4. Biologically Active Compounds From Caribbean Sponges

    … and structure elucidation of a number of 1,2-dioxolane and 1,2 dioxane acids and esters from two caribbean sponges is described. Interest in these compounds was motivated by the acid's pharmacological activities when tested in vitro against various gram positive bacteria, yeasts and fungi. The …

    uiuc Repository record for Biologically Active Compounds From Caribbean Sponges (opens in a new tab)

  5. Mechanisms of Chemiluminescence

    … of 4-bromo-3-hydroxy-3,5,5-trimethyl-1,2-dioxolane. Thermal decomposition of this dissymmetric dioxetane to acetone and methylglyoxal proceeds with an activation energy of 26.0 (+OR-) 1 kcal/mol and a log A of 14.2. The enthalpy of activation and entropy of activation were determined to be …

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