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  2. Suzuki reaction - Wikipedia

    en.wikipedia.org/wiki/Suzuki_reaction

    The Suzuki reaction or Suzuki coupling is an organic reaction that uses a palladium complex catalyst to cross-couple a boronic acid to an organohalide. [1] [2] [3] It was first published in 1979 by Akira Suzuki, and he shared the 2010 Nobel Prize in Chemistry with Richard F. Heck and Ei-ichi Negishi for their contribution to the discovery and development of noble metal catalysis in organic ...

  3. Norio Miyaura - Wikipedia

    en.wikipedia.org/wiki/Norio_Miyaura

    Norio Miyaura (宮浦憲夫, Miyaura Norio) was a Japanese organic chemist. He was a professor of graduate chemical engineering at Hokkaido University. [1] His major accomplishments surrounded his work in cross-coupling reactions / conjugate addition reactions of organoboronic acids (for C-C bond-forming reactions) and addition / coupling reactions of diborons and boranes (to synthesize ...

  4. Cross-coupling reaction - Wikipedia

    en.wikipedia.org/wiki/Cross-coupling_reaction

    Cross-coupling reactions are important for the production of pharmaceuticals, [4] examples being montelukast, eletriptan, naproxen, varenicline, and resveratrol. [21] with Suzuki coupling being most widely used. [22] Some polymers and monomers are also prepared in this way. [23]

  5. Bioconjugation - Wikipedia

    en.wikipedia.org/wiki/Bioconjugation

    The nucleophilic lysine residue is commonly targeted site in protein bioconjugation, typically through amine-reactive N-hydroxysuccinimidyl (NHS) esters. [3] To obtain optimal number of deprotonated lysine residues, the pH of the aqueous solution must be below the pKa of the lysine ammonium group, which is around 10.5, so the typical pH of the reaction is about 8 and 9.

  6. Miyaura borylation - Wikipedia

    en.wikipedia.org/wiki/Miyaura_borylation

    The Miyaura borylation has shown to work for: Alkyl halides, [ 2 ] aryl halides, [ 1 ] [ 3 ] [ 4 ] aryl halides using tetrahydroxydiboron , [ 5 ] aryl halides using bis-boronic acid, [ 6 ] aryl triflates , [ 7 ] aryl mesylates , [ 8 ] vinyl halides, [ 9 ] vinyl halides of α,β-unsaturated carbonyl compounds, [ 10 ] and vinyl triflates.

  7. Akira Suzuki - Wikipedia

    en.wikipedia.org/wiki/Akira_Suzuki

    Akira Suzuki (鈴木 章, Suzuki Akira, born September 12, 1930) is a Japanese chemist and Nobel Prize Laureate (2010), who first published the Suzuki reaction, the organic reaction of an aryl- or vinyl-boronic acid with an aryl- or vinyl-halide catalyzed by a palladium(0) complex, in 1979.

  8. Neural synchrony - Wikipedia

    en.wikipedia.org/wiki/Neural_Synchrony

    Early conceptualizations of neural synchrony, mostly from the Hasson Lab at Princeton University, were motivated by models of stimulus-to-brain coupling. In these models, aspects of the physical environment emit mechanical, chemical, and electromagnetic signals, which the brain receives and translates into electrical impulses that guide our ...

  9. Modern Hopfield network - Wikipedia

    en.wikipedia.org/wiki/Modern_Hopfield_Network

    Model A reduces to the models studied in [3] [4] depending on the choice of the activation function, model B reduces to the model studied in, [1] model C reduces to the model of. [ 5 ] General systems of non-linear differential equations can have many complicated behaviors that can depend on the choice of the non-linearities and the initial ...