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    Micellar promoted alkenes isomerization in water mediated by a cationic half-sandwich Ru(II) complex

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    Micellar media in water provide a simple and efficient environment to favor the double bond isomerization of terminal alkenes catalyzed by the cationic half-sandwich complex 1 at 95 °C. The micellar medium favors both catalyst dissolution in water by means of ion-pairing with the preferred anionic surfactants as well as substrate dissolution thus favoring its conversion into products

    Organic micropollutants (PAHs, PCBs, Pesticides) in seaweeds of the lagoon of Venice

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    Samples of seven genera of seaweeds (Ulva, Gracilaria, Porphyra, Grateloupia, Undaria, Fucus and Cystoseira), which can be used as environmental biomonitors and in several applications like human alimentation, animal feeding and cosmetics, were collected in four sampling sites in the Lagoon of Venice in spring and autumn 1999 with the aim of determining the contamination due to organic micropollutants (polychlorinated biphenyls. PCBs; chlorinated pesticides; polycyclic aromatic hydrocarbons, PAHs). On an average, most of the considered species were contaminated especially by PAHs (up to 56 ng g(-1) dry wt. (dw)) whereas concentrations of PCBs and pesticides in macroalgal tissues were significantly correlated and did not exceed 5 ng g-1 dw. Among the studied genera the most contaminated by PAHs were Ulva, Undaria and Cystoseira. The highest concentrations of PCBs and pesticides were found in Cystoseira, Fucus and Gracilaria. The least contaminated genus was Porphyra. Although macroalgal specimens were sampled in differently contaminated areas placed from the mainland to the Lido Lagoon mouth, no quantitatively meaningful differences of concentrations were found among the sampling stations. (C) 2003 Editions scientifiques et medicales Elsevier SAS and Ifremer/CNRS/IRD. All rights reserved

    Organocatalytic Enantioselective Epoxidation of\ud Some Aryl-Substituted Vinylidenebisphosphonate\ud Esters: On the Way to Chiral Anti-Osteoporosis Drugs

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    The synthesis of a new class of epoxide derivatives from prochiral vinylidene bisphosphonate (VBP) precursors is reported using hydrogen peroxide as the terminal oxidant. The reaction is carried out using a series of possible organic catalysts having a basic character, the best results being observed using quinine and sparteine. These catalysts not only provide from good to excellent epoxide yields with a large variety of VBPs but also interesting enantioselectivities in the 67-96% ee range at least in the case of the Ph and m-MeO-Ph VBP derivatives opening the way to a number of chiral anti-osteoporosis potentially active pharmaceutical ingredient

    Supramolecular Encapsulation of Neutral Diazoacetate Esters and Catalyzed 1,3-Dipolar Cycloaddition Reaction by a Self-Assembled Hexameric Capsule

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    Diazoacetate esters proved to be suitable neutral guests for the self-assembled resorcin[4]arene hexameric capsule. The hydrogen- bonded supramolecular host catalyzed the 1,3-dipolar cycloaddition reaction between diazoacetate esters and electron- poor alkenes such as acrolein, acrylonitrile, crotonaldehyde, trans-2-hexenal, methyl, and butyl acrylate, which led to the corresponding 4,5-dihydro-1H-pyrazole derivatives. The cycloaddition reaction occurred within the cavity of the capsule. In fact, substantial inhibition of the catalytic activity was observed by employing tetraethylammonium tetrafluoroborate characterized by greater affinity for the hexameric capsule as a competitive guest; its presence inhibited access of the substrates. The 1,3-dipolar cycloaddition reaction between diazoacetate esters and acrylate esters of different lengths showed a significant degree of substrate selectivity owing to the encapsulation of the reagents before the cycloaddition reaction
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