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  2. E1cB-elimination reaction - Wikipedia

    en.wikipedia.org/wiki/E1cB-elimination_reaction

    Deuterium exchange and a deuterium kinetic isotope effect can help distinguish among E1cB rev, E1cB anion, and E1cB irr. If the solvent is protic and contains deuterium in place of hydrogen (e.g., CH 3 OD), then the exchange of protons into the starting material can be monitored.

  3. Elimination reaction - Wikipedia

    en.wikipedia.org/wiki/Elimination_reaction

    Elimination reaction of cyclohexanol to cyclohexene with sulfuric acid and heat [1] An elimination reaction is a type of organic reaction in which two substituents are removed from a molecule in either a one- or two-step mechanism. [2] The one-step mechanism is known as the E2 reaction, and the two-step mechanism is known as the E1 reaction ...

  4. Adenylosuccinate lyase - Wikipedia

    en.wikipedia.org/wiki/Adenylosuccinate_lyase

    Adenylosuccinate lyase (ASL) is an enzyme that catalyzes two reactions in the de novo purine biosynthetic pathway. In both reactions it uses an E1cb elimination reaction mechanism to cleave fumarate off of the substrate. In the first reaction, ASL converts 5-aminoimidazole- (N-succinylocarboxamide) ribotide (SAICAR) to 5-aminoimidazole-4 ...

  5. Deuterated drug - Wikipedia

    en.wikipedia.org/wiki/Deuterated_drug

    A deuterated drug is a small molecule medicinal product in which one or more of the hydrogen atoms in the drug molecule have been replaced by its heavier stable isotope deuterium. Because of the kinetic isotope effect, deuterium-containing drugs may have significantly lower rates of metabolism, and hence a longer half-life. [1] [2] [3]

  6. Ei mechanism - Wikipedia

    en.wikipedia.org/wiki/Ei_mechanism

    In organic chemistry, the E i mechanism (Elimination Internal/Intramolecular), also known as a thermal syn elimination or a pericyclic syn elimination, is a special type of elimination reaction in which two vicinal (adjacent) substituents on an alkane framework leave simultaneously via a cyclic transition state to form an alkene in a syn elimination. [1]

  7. Aneutronic fusion - Wikipedia

    en.wikipedia.org/wiki/Aneutronic_fusion

    Although the deuterium reactions (deuterium + 3 He and deuterium + 6 lithium) do not in themselves release neutrons, in a fusion reactor the plasma would also produce D–D side reactions that result in reaction product of 3 He plus a neutron. Although neutron production can be minimized by running a plasma reaction hot and deuterium-lean, the ...

  8. The Hope and Hype of Fusion Energy, Explained - AOL

    www.aol.com/news/hope-hype-fusion-energy...

    Early this month, South Korea’s KFE (Korean Institute of Fusion Energy) announced it had sustained the kind of high temperatures that fusion reactions require—100 million degrees Celsius ...

  9. More O'Ferrall–Jencks plot - Wikipedia

    en.wikipedia.org/wiki/More_O'Ferrall–Jencks_plot

    These plots were first introduced in a 1970 paper by R. A. More O’Ferrall to discuss mechanisms of β-eliminations [2] and later adopted by W. P. Jencks in an attempt to clarify the finer details involved in the general acid-base catalysis of reversible addition reactions to carbon electrophiles such as the hydration of carbonyls.