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  2. Electrophilic amination - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_amination

    A nitrogen bound to both a good electrofuge and a good nucleofuge is known as a nitrenoid (for its resemblance to a nitrene). [2] Nitrenes lack a full octet of electrons are thus highly electrophilic; nitrenoids exhibit analogous behavior and are often good substrates for electrophilic amination reactions.

  3. Michael addition reaction - Wikipedia

    en.wikipedia.org/wiki/Michael_Addition_Reaction

    Others, however, insist that such a usage is an abuse of terminology, and limit the Michael addition to the formation of carbon–carbon bonds through the addition of carbon nucleophiles. The terms oxa-Michael reaction and aza-Michael reaction [2] have been used to refer to the 1,4-addition of oxygen and nitrogen nucleophiles, respectively. The ...

  4. Petasis reaction - Wikipedia

    en.wikipedia.org/wiki/Petasis_reaction

    When used as nitrogen nucleophiles, amino acids can furnish various iminodicarboxylic acid derivatives. High diastereoselectivity is usually observed, and the newly formed stereocenter usually share the same configuration with the starting amino acid. This reaction works well in highly polar solvents (ex. water, ethanol, etc.).

  5. Metal nitrosyl complex - Wikipedia

    en.wikipedia.org/wiki/Metal_nitrosyl_complex

    Since nitrogen is more electronegative than carbon, metal-nitrosyl complexes tend to be more electrophilic than related metal carbonyl complexes. Nucleophiles often add to the nitrogen. [2] The nitrogen atom in bent metal nitrosyls is basic, thus can be oxidized, alkylated, and protonated, e.g.: (Ph 3 P) 2 (CO)ClOsNO + HCl → (Ph 3 P) 2 (CO ...

  6. Nucleophile - Wikipedia

    en.wikipedia.org/wiki/Nucleophile

    A hydroxide ion acting as a nucleophile in an S N 2 reaction, converting a haloalkane into an alcohol. In chemistry, a nucleophile is a chemical species that forms bonds by donating an electron pair. All molecules and ions with a free pair of electrons or at least one pi bond can act as nucleophiles. Because nucleophiles donate electrons, they ...

  7. 4 Dividend Stocks to Double Up on Right Now - AOL

    www.aol.com/finance/4-dividend-stocks-double-now...

    Data source: Ned Davis Research and Hartford Funds. Here are four dividend payers to consider for your long-term stock portfolio: 1. Pfizer. Pfizer (NYSE: PFE) is a more familiar name than it was ...

  8. ANRORC mechanism - Wikipedia

    en.wikipedia.org/wiki/ANRORC_mechanism

    The ANRORC mechanism in organic chemistry describes a special type of substitution reaction.ANRORC stands for Addition of the Nucleophile, Ring Opening, and Ring Closure in nucleophilic attack on ring systems [1] [2] [3] and it helps to explain product formation and distribution in some nucleophilic substitutions especially in heterocyclic compounds.

  9. Elon Musk calls for 'deleting' the Consumer Financial ... - AOL

    www.aol.com/finance/elon-musk-calls-deleting...

    President-elect Trump's adviser on government efficiency, Elon Musk, called for eliminating the Consumer Financial Protection Bureau.