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  2. Phenylacetylene - Wikipedia

    en.wikipedia.org/wiki/Phenylacetylene

    Phenylacetylene is a prototypical terminal acetylene, undergoing many reactions expected of that functional group. It undergoes semi hydrogenation over Lindlar catalyst to give styrene . In the presence of base and copper(II) salts, it undergoes oxidative coupling to give diphenylbutadiyne . [ 6 ]

  3. Multiple chemical sensitivity - Wikipedia

    en.wikipedia.org/wiki/Multiple_chemical_sensitivity

    Symptoms affect a variety of different organ systems. Different people have different symptoms and different affected systems, but cognitive and neurologic symptoms (e.g., headache and brain fog) are common, as are systemic symptoms (e.g., fatigue). [5]

  4. Stevens–Johnson syndrome - Wikipedia

    en.wikipedia.org/wiki/Stevens–Johnson_syndrome

    Stevens–Johnson syndrome (SJS) is a type of severe skin reaction. [1] Together with toxic epidermal necrolysis (TEN) and Stevens–Johnson/toxic epidermal necrolysis (SJS/TEN) overlap, they are considered febrile mucocutaneous drug reactions and probably part of the same spectrum of disease, with SJS being less severe.

  5. Glaser coupling - Wikipedia

    en.wikipedia.org/wiki/Glaser_coupling

    The Hay coupling is variant of the Glaser coupling. It relies on the TMEDA complex of copper(I) chloride to activate the terminal alkyne. Oxygen (air) is used in the Hay variant to oxidize catalytic amounts of Cu(I) to Cu(II) throughout the reaction, as opposed to a stoichiometric amount of Cu(II) used in the Eglington variant. [7]

  6. Chemotherapy-induced acral erythema - Wikipedia

    en.wikipedia.org/wiki/Chemotherapy-induced_acral...

    Symptoms resolve 1–2 weeks after cessation of chemotherapy. [6] The range is 1–5 weeks, so it has recovered by the time the next cycle is due. Healing occurs without scarring unless there has been skin ulceration or necrosis. With each subsequent cycle of chemotherapy, the reaction will appear more quickly, be more severe and will take ...

  7. Kumada coupling - Wikipedia

    en.wikipedia.org/wiki/Kumada_coupling

    In organic chemistry, the Kumada coupling is a type of cross coupling reaction, useful for generating carbon–carbon bonds by the reaction of a Grignard reagent and an organic halide. The procedure uses transition metal catalysts , typically nickel or palladium, to couple a combination of two alkyl , aryl or vinyl groups .

  8. Peanuts! Get your peanuts! Kids who eat them early are ... - AOL

    www.aol.com/news/peanuts-peanuts-kids-eat-them...

    After tracking hundreds of children, researchers conclude that babies who eat peanut protein early and often in their first five years of life are 71% less likely to be allergic to peanuts at age 12.

  9. Sonogashira coupling - Wikipedia

    en.wikipedia.org/wiki/Sonogashira_coupling

    The reaction medium must be basic to neutralize the hydrogen halide produced as the byproduct of this coupling reaction, so alkylamine compounds such as triethylamine and diethylamine are sometimes used as solvents, but also DMF or ether can be used as solvent. Other bases such as potassium carbonate or cesium carbonate are occasionally used.