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  2. Carbon–hydrogen bond activation - Wikipedia

    en.wikipedia.org/wiki/Carbon–hydrogen_bond...

    On the category of oxidative addition, M. L. H. Green in 1970 reported on the photochemical insertion of tungsten (as a Cp 2 WH 2 complex) in a benzene CH bond [7] and George M. Whitesides in 1979 was the first to carry out an intramolecular aliphatic CH activation [8] Fujiwara's palladium- and copper-catalyzed C-H functionalization

  3. N,N'-Dicyclohexylcarbodiimide - Wikipedia

    en.wikipedia.org/wiki/N,N'-Dicyclohexylcarbodiimide

    Of academic interest, palladium acetate, iodine, and oxygen can be used to couple cyclohexyl amine and cyclohexyl isocyanide. [5] Yields of up to 67% have been achieved using this route: C 6 H 11 NC + C 6 H 11 NH 2 + O 2 → (C 6 H 11 N) 2 C + H 2 O. DCC has also been prepared from dicyclohexylurea using a phase transfer catalyst.

  4. Ga-68-Trivehexin - Wikipedia

    en.wikipedia.org/wiki/Ga-68-Trivehexin

    For radiolabeling, the pH of the 68 Ga containing generator eluate has to be raised from its initial value (depending on HCl concentration, pH 11.5) to pH 2–3.5 [11] using suitable buffers, such as sodium acetate.

  5. N,N'-Diisopropylcarbodiimide - Wikipedia

    en.wikipedia.org/wiki/N,N'-Diisopropylcarbodiimide

    C 7 H 14 N 2: Molar mass: 126.203 g·mol −1 Appearance Liquid Density: 0.806 g/mL Boiling point: 145 to 148 °C (293 to 298 °F; 418 to 421 K) Hazards GHS labelling:

  6. N-Hydroxysuccinimide - Wikipedia

    en.wikipedia.org/wiki/N-Hydroxysuccinimide

    A common way to synthesize an NHS-activated acid is to mix NHS with the desired carboxylic acid and a small amount of an organic base in an anhydrous solvent. A coupling reagent such as dicyclohexylcarbodiimide (DCC) or 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) is then added to form a highly reactive activated acid intermediate.

  7. Electrophilic aromatic directing groups - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    For nitration, for example, fluorine directs strongly to the para position because the ortho position is inductively deactivated (86% para, 13% ortho, 0.6% meta). On the other hand, iodine directs to ortho and para positions comparably (54% para and 45% ortho, 1.3% meta). [12]

  8. Sodium nonanoyloxybenzenesulfonate - Wikipedia

    en.wikipedia.org/wiki/Sodium_nonanoyloxybenzenes...

    NOBS is the main bleach activator used in the U.S.A. and Japan. [4] Compared to TAED, which is the predominant bleach activator used in Europe, NOBS is efficient at much lower temperatures. At 20 °C NOBS is 100 times more soluble than TAED in water. [5]

  9. Activator (phosphor) - Wikipedia

    en.wikipedia.org/wiki/Activator_(phosphor)

    In phosphors and scintillators, the activator is the element added as dopant to the crystal of the material to create desired type of nonhomogeneities. In luminescence , only a small fraction of atoms, called emission centers or luminescence centers , emit light.