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Showing 1 to 7 of 7 for “"Diazirines"”.

  1. Utilisation des diazirines comme source d'azote électrophile pour la synthèse d'hydrazines et d'hétérocycles

    … la faible diversité des produits obtenus. Les diazirines présentent un fort potentiel pour être utilisées comme alternative à ces préparations, puisque ces molécules peuvent réagir avec des nucléophiles pour donner les diaziridines substituées correspondantes, puis être hydrolysées pour …

    sherbrooke Repository record for Utilisation des diazirines comme source d'azote électrophile pour la synthèse d'hydrazines et d'hétérocycles (opens in a new tab)

  2. Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile

    … différent sera traité, celui de la chimie des diazirines. Actuellement, les diazirines sont utilisées principalement comme source de carbènes, mais dans cet ouvrage il sera démontré que les diazirines peuvent agir comme source d'azote électrophile. Cette propriété est très intéressante et sera …

    sherbrooke Repository record for Développement de catalyseurs pour la réaction d'halolactonisation énantiosélective et valorisation de diazirines comme source d'azote électrophile (opens in a new tab)

  3. 1. Neighboring group participation in some sulfides and sulfoxides. 2. Nuclear magnetic resonance studies of diazirines

    Made available in DSpace on 2014-12-09T17:34:59Z (GMT). No. of bitstreams: 1 6500931.pdf: 7504343 bytes, checksum: c4c2969d6fafd613bfead3ffdef229a1 (MD5) Previous issue date: 1964

    uiuc Repository record for 1. Neighboring group participation in some sulfides and sulfoxides. 2. Nuclear magnetic resonance studies of diazirines (opens in a new tab)

  4. Photochemistry of 5-Membered Heteroaryl(trifluoromethyl)carbenes in Low Temperature Matrices

    … led us to a new realm of UV-vis transparent diazirines, which behave as normal diazirine photochemically, but have very weak n<em>f</em>à<em>f</em>x<em>f</em>nabsorptions which are not visible in experimental UV-vis spectra. Also, we were able to synthesize diazirine precursors of both 2- and …

    unr Repository record for Photochemistry of 5-Membered Heteroaryl(trifluoromethyl)carbenes in Low Temperature Matrices (opens in a new tab)

  5. MODIFIED BODIPY PROBES TO EXPLORE PEROXISOME FUNCTION

    … and para methoxy substituted trifluoromethyl diazirines, were attempted these were not successful. In an alternative approach, 4-benzoylphenylboronic acid was used as the pro-photoaffinity labelling residue. This could successfully be coupled with iodo-BODIPY for future use as cell-labelling …

    durham Repository record for MODIFIED BODIPY PROBES TO EXPLORE PEROXISOME FUNCTION (opens in a new tab)

  6. Matrix Isolation of Aryl(trifluoromethyl)carbenes, Heteroaryl(trifluoromethyl)carbenes and Phenylbis(trifluoromethyl)carbenes

    … The 1- and 2-naphthyl(trifluoromethyl)diazirines, the precursors of 1- and 2-naphthyl(trifluoromethyl)carbenes, have dissimilar geometric structures leading to differentUV/Vis absorptions. In the studied pyridyl(trifluoromethyl)carbenes, 4-pyridyl(trifluoromethyl)carbene was the most …

    unr Repository record for Matrix Isolation of Aryl(trifluoromethyl)carbenes, Heteroaryl(trifluoromethyl)carbenes and Phenylbis(trifluoromethyl)carbenes (opens in a new tab)

  7. Pioneering investigations into organometallic electrochemistry

    … are also reported. In chapter 5, the use of diazirines as carbene precursors for carbon surface modification is investigated, via the synthesis and characterisation of diazirine derivatised cymantrene and cyrhetrene. The surface modification of glassy carbon electrodes was attempted via …

    east-anglia Repository record for Pioneering investigations into organometallic electrochemistry (opens in a new tab)