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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. Surface activated bonding - Wikipedia

    en.wikipedia.org/wiki/Surface_activated_bonding

    Surface activated bonding (SAB) is a non-high-temperature wafer bonding technology with atomically clean and activated surfaces. Surface activation prior to bonding by using fast atom bombardment is typically employed to clean the surfaces.

  4. Enzyme activator - Wikipedia

    en.wikipedia.org/wiki/Enzyme_activator

    The N-terminal acts as an allosteric regulator of C-terminal; the C-terminal is the only one involved in the catalytic activity. HK-I is regulated by the concentration of G6P, where G6P acts as a feedback inhibitor. At low G6P concentration, HK-I is activated; at high G6P concentration, the HK-I is inhibited. [1]

  5. 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 ]

  6. Tetraacetylethylenediamine - Wikipedia

    en.wikipedia.org/wiki/Tetraacetylethylenediamine

    Tetraacetylethylenediamine, commonly abbreviated as TAED, is an organic compound with the formula (CH 3 C(O)) 2 NCH 2 CH 2 N(C(O)CH 3) 2. It is a white solid commonly used as a bleach activator in laundry detergents and in the production of paper pulp. TAED is synthesized through the acetylation of ethylenediamine.

  7. Pleckstrin homology domain - Wikipedia

    en.wikipedia.org/wiki/Pleckstrin_homology_domain

    This domain can bind phosphatidylinositol lipids within biological membranes (such as phosphatidylinositol (3,4,5)-trisphosphate and phosphatidylinositol (4,5)-bisphosphate), [8] and proteins such as the βγ-subunits of heterotrimeric G proteins, [9] and protein kinase C. [10]

  8. Carbamoyl phosphate synthetase I - Wikipedia

    en.wikipedia.org/wiki/Carbamoyl_phosphate_syn...

    CPSI is regulated by N-acetylglutamate which acts as an obligate allosteric activator of CPS1. NAG, by binding to domain L4, triggers changes in the A-loop and in Arg1453 that result in changing interactions with the T′-loop of domain L3, which reorganizes completely from a β-hairpin in the apo form to a widened loop in the ligand-bound form ...

  9. N,N'-Diisopropylcarbodiimide - Wikipedia

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

    [1] [2] As a liquid, it is easier to handle than the commonly used N,N ′-dicyclohexylcarbodiimide, a waxy solid. In addition, N , N ′ -diisopropylurea, its byproduct in many chemical reactions, is soluble in most organic solvents , a property that facilitates work-up .

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