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Showing 1 to 20 of 65 for “"azides"”.

  1. The Photochemistry of 3- and 4-Nitro Phenyl Azides

    The photochemistry of 4-nitro and 3-nitrophenyl azides in inert and reactive solvents was examined. Photolysis of nitrophenyl azides in solution at room temperature or in a frozen glass at 77 K gives triplet nitrenes. The products of the reaction of triplet nitrenes depend on the power of the light …

    uiuc Repository record for The Photochemistry of 3- and 4-Nitro Phenyl Azides (opens in a new tab)

  2. The photolysis and co-irradiated decomposition of barium and strontium azides

    The effect of ultraviolet radiation on sieved powders and pellets of barium azide in the temperature range 27,0° - 135,0°C and of strontium azide in the temperature range 30,0° - l35,0°C has been studied. Decompositions in the temperature range 27,0°- 100,0°C for barium azide and 30,0° - 90,0°C for …

    cape-town Repository record for The photolysis and co-irradiated decomposition of barium and strontium azides (opens in a new tab)

  3. Aryl Azides as Photoaffinity Labels for Estrogen Binding Proteins in the Rat Uterus

    Made available in DSpace on 2014-12-10T23:02:06Z (GMT). No. of bitstreams: 1 7511579.pdf: 5060650 bytes, checksum: a860aa18e8d08ca9410b303e913a27d0 (MD5) Previous issue date: 1974

    uiuc Repository record for Aryl Azides as Photoaffinity Labels for Estrogen Binding Proteins in the Rat Uterus (opens in a new tab)

  4. The photolysis of calcium, barium, strontium and lithium azides and the co-irradiated decomposition of calcium azide

    … powdered calcium, barium, strontium and lithium azides in the temperature range -80,0° - 35,0°C has been studied. Powdered and pelleted calcium azide was also irradiated with ultraviolet radiation in the temperature range 35,0° - 90,0°C and powdered lithium azide in the temperature range 24,0° - …

    cape-town Repository record for The photolysis of calcium, barium, strontium and lithium azides and the co-irradiated decomposition of calcium azide (opens in a new tab)

  5. Synthetic and mechanistic investigation of new radical processes: reaction of organic azides with group-XIII Lewis acids

    … of organic (alkyl, aryl, acyl, solfonyl) azides. The new approach entails mild reaction conditions and provides high yields of the corresponding amines and amides, also showing high degrees of selectivity. The system dichloroindium hydride / azides can be utilised in fivemembered ring …

    bologna Repository record for Synthetic and mechanistic investigation of new radical processes: reaction of organic azides with group-XIII Lewis acids (opens in a new tab)

  6. The Chemistry of Aroyl Azides in Piperidine- and Steroid-Separated Bichromophoric System: Photoinduced Long-Distance Intramolecular Electron Transfer Reactions

    The photochemistry and photophysics of piperidine- and steroid- separated bichromophoric systems containing an aroyl azide as the electron acceptor and secondary aromatic amines as the electron donors was examined. We report the first example of unique photochemical reactivity associated with …

    uiuc Repository record for The Chemistry of Aroyl Azides in Piperidine- and Steroid-Separated Bichromophoric System: Photoinduced Long-Distance Intramolecular Electron Transfer Reactions (opens in a new tab)

  7. Synthetic methodologies toward the functionalization of benzhydrols and carbohydrates

    Organoazides are highly versatile substrates that are often used as precursors to triazoles, amides, amines and imines. As dipolar functional groups, azides are routinely exploited in chemical biology as a means to append biomarkers onto macromolecules via cycloaddition reactions. Furthermore, the …

    uoit Repository record for Synthetic methodologies toward the functionalization of benzhydrols and carbohydrates (opens in a new tab)

  8. Part One: Photochemistry of Aryl Azides. Chemical Properties of the Transient Intermediates. Part Two: Thermolysis of an Endoperoxide. Generation of an O-Xylylene Peroxide (Nitrene)

    … The products of direct photolysis of the aryl azides can depend dramatically on the concentration of the azide and on the power of the light source. Direct irradiation gives the triplet aryl nitrenes, with relatively long-lived singlet-state precursors. The structures of these intermediates and …

    uiuc Repository record for Part One: Photochemistry of Aryl Azides. Chemical Properties of the Transient Intermediates. Part Two: Thermolysis of an Endoperoxide. Generation of an O-Xylylene Peroxide (Nitrene) (opens in a new tab)

  9. Design, synthesis, and biochemical evaluation of novel photoaffinity labeling reagents for the estrogen and progesterone receptors

    … attachment to ER from rat uterus. Both azides 1 and 2 demonstrate high binding affinity for ER as determined by both a competitive binding assay (relative binding affinities: estradiol = 100; TFAA = 9.3; PAA = 66) and a direct binding assay (K$\sb{\rm d}$: estradiol = 0.24 nM; TFAA = …

    uiuc Repository record for Design, synthesis, and biochemical evaluation of novel photoaffinity labeling reagents for the estrogen and progesterone receptors (opens in a new tab)

  10. Characterizing triplet azo biradical and corannulene- halogen complexes by laser flash photolysis

    … systems: 1) the photolysis of aryl azides in solution and in solid-state 2) the photo-reaction of corannulene in halogenated solvents.</p><p>Singlet aryl nitrene was formed upon irradiation of aryl azides, and the singlet nitrene could decay by intersystem-crossing to form triplet …

    ohiolink Repository record for Characterizing triplet azo biradical and corannulene- halogen complexes by laser flash photolysis (opens in a new tab)

  11. Reaction of allene with phenyl azide

    … gain greater insight into the reaction of aryl azides with allenes.

    u-pacific Repository record for Reaction of allene with phenyl azide (opens in a new tab)

  12. Lewis acid catalysis in organic synthesis

    … been developed for 1,3-dipolar cycloaddition of azides to terminal alkynes using CuCl-RTIL. This catalytical system gives only 1,4-disubstituted 1,2,3-triazoles. Reactions of Alkyl and aryl azides with a variety of terminal alkynes were successfully catalyzed using CuCl-RTIL catalytic system. …

    must-thes Repository record for Lewis acid catalysis in organic synthesis (opens in a new tab)

  13. Regioselective Synthesis of Glycosaminoglycan Analogs

    … followed by azide displacement to introduce azides as the GAG amine precursors. The resulting 6-N3 cellulose acetate was then saponified to liberate 6-OH groups, followed by subsequent (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) oxidation of the liberated primary hydroxyl groups to …

    vt Repository record for Regioselective Synthesis of Glycosaminoglycan Analogs (opens in a new tab)

  14. Stereoselective alkylations and rearrangements of chiral phosphonic and phosphinic acid derivatives

    … ($\geq$99.9% e.e.) phosphonic and phosphinic azides were prepared and photolyzed in methanol to effect the phosphorus analogues of the carbonyl-Curtius rearrangement. These studies showed that carbon migration in the phosphinoyl-Curtius rearrangement proceeds with 99% net retention of …

    uiuc Repository record for Stereoselective alkylations and rearrangements of chiral phosphonic and phosphinic acid derivatives (opens in a new tab)

  15. Dielectric Breakdown of Silver Azide

    The breakdown of single crystals of heavy metal azides has been investigated. In silver azide, the low-field conduction is by mobile interstitial cations and their enthalpies ,of formation and hopping have been determined from the Arrhenius plot of the conductivity. Based on AC conductivity · …

    cambridge Repository record for Dielectric Breakdown of Silver Azide (opens in a new tab)

  16. Controlled metabolic cell labeling and bioorthogonal click chemistry for cancer targeting

    … label cell surface with chemical groups (e.g., azides) only in the presence of either exogenous triggers (ultraviolet (UV)) or endogenous triggers (H2O2, tumor hypoxia, NAD(P)H dehydrogenase quinone 1 (NQO1), and histone deacetylase (HDAC)/cathepsin L (CTSL)). Among them, HDAC/CTSL-responsive …

    uiuc Repository record for Controlled metabolic cell labeling and bioorthogonal click chemistry for cancer targeting (opens in a new tab)

  17. Synthesis of N-Heterocycles and Thiocines via Electrophilic Divalent Reactive Intermediates

    … My research has focused on using aryl amines and azides as the N-atom source to synthesize these complex organic scaffolds that possess biological activity such as dibenzazepines, benzimidazoles, and 3H-indoles by accessing electrophilic divalent intermediates. I found that exposure of …

    uic

  18. STUDY OF CLICK CHEMISTRY: WORKING TOWARDS ‘CLICKING’ A NON-STEROIDAL ANTI-INFLAMMATORY TO AN APOPTOSIS INHIBITOR Q-VD-OPH

    … 1,2,3-triazole forming reaction between azides and terminal alkynes has contributed to drug discovery due to the high degree of dependability, efficiency, specificity and biocompatibility of the reactions and products. Using this well-known click chemistry reaction, a non-steroidal …

    ohiolink Repository record for STUDY OF CLICK CHEMISTRY: WORKING TOWARDS ‘CLICKING’ A NON-STEROIDAL ANTI-INFLAMMATORY TO AN APOPTOSIS INHIBITOR Q-VD-OPH (opens in a new tab)

  19. Part I. Aromatic Fluorinations for Fluorine-18 Labeling of Estrogens. Part Ii. Bromodesilylation-Potential Method for Regiospecific Radiobromination of Aromatic Systems. Part Iii. Synthesis of Isohexestrol and Isohexestrol Derivatives

    … fluorination methods, the decomposition of aryl azides and the decomposition of aryl triazenes, were investigated as methods potentially suitable for fluorine-18 labeling of estrogens. The aryl triazene method gives moderate yields in many systems, but fails with ortho methoxy or …

    uiuc Repository record for Part I. Aromatic Fluorinations for Fluorine-18 Labeling of Estrogens. Part Ii. Bromodesilylation-Potential Method for Regiospecific Radiobromination of Aromatic Systems. Part Iii. Synthesis of Isohexestrol and Isohexestrol Derivatives (opens in a new tab)

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