24 research outputs found

    Low incidence of SARS-CoV-2, risk factors of mortality and the course of illness in the French national cohort of dialysis patients

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    Synthesis of homopropargylamines from 2-cyanoazetidines

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    International audienceMild generation of vinylidene carbene from α-amino nitrile is the basis of a new synthesis of homopropargylamines

    Novel liposaccharide conjugates for drug and peptide delivery

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    Sugar-lipid conjugates with general structure 1-4 were prepared by coupling amino sugars with N-Boc-protected lipoamino acids and oligomers. Conjugates with general structure 5 were also prepared from glucuronic acid and methyl 2-aminohexadecanoate. The physicochemical properties of the conjugates were modified by varying the nature and number of sugars or the number of lipoamino acids or their alkyl chain length. The ability of the liposaccharides to aggregate was examined. These preliminary experiments have demonstrated the ability of the liposaccharides to form particulate systems per se and also their ability to be incorporated into conventional liposomal systems. The structure of the respective liposaccharides and the molar ratio of liposaccharide to dimyristoyl lecithin and cholesterol were found to have a profound effect on the type of colloidal systems produced

    Aza-[2,3]-Wittig Sigmatropic Rearrangement of Allylic Tertiary Amines: A Successful Example with High Chirality Transfer

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    We report herein a successful example of an aza-[2,3]-Wittig rearrangement in an allylic tertiary <i>N,N</i>-dibenzyl amine derived from (<i>S</i>)-alaninol or (<i>S</i>)-isoleucinol. This reaction occurs upon metalation at the benzylic position with a mixture of butyllithium/diisopropylamine/potassium <i>t</i>-butoxide and proceeds with a high 1,3 transfer of chirality

    Aza-[2,3]-Wittig Sigmatropic Rearrangement of Allylic Tertiary Amines: A Successful Example with High Chirality Transfer

    No full text
    We report herein a successful example of an aza-[2,3]-Wittig rearrangement in an allylic tertiary <i>N,N</i>-dibenzyl amine derived from (<i>S</i>)-alaninol or (<i>S</i>)-isoleucinol. This reaction occurs upon metalation at the benzylic position with a mixture of butyllithium/diisopropylamine/potassium <i>t</i>-butoxide and proceeds with a high 1,3 transfer of chirality
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