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  2. Organic base - Wikipedia

    en.wikipedia.org/wiki/Organic_base

    An organic base is an organic compound which acts as a base. Organic bases are usually, but not always, proton acceptors. They usually contain nitrogen atoms, which can easily be protonated. For example, amines or nitrogen-containing heterocyclic compounds have a lone pair of electrons on the nitrogen atom and can thus act as proton acceptors ...

  3. List of reagents - Wikipedia

    en.wikipedia.org/wiki/List_of_reagents

    a strong base; deprotonates ketones and esters to generate enolate derivative Sodium borohydride: a versatile reducing agent; converts ketones and aldehydes to alcohols Sodium chlorite: in organic synthesis, used for the oxidation of aldehydes to carboxylic acids Sodium hydride: a strong base used in organic synthesis Sodium hydroxide

  4. N,N-Diisopropylethylamine - Wikipedia

    en.wikipedia.org/wiki/N,N-Diisopropylethylamine

    DIPEA is a sterically hindered organic base that is commonly employed as a proton scavenger. Thus, like 2,2,6,6-tetramethylpiperidine and triethylamine, DIPEA is a good base but a poor nucleophile, DIPEA has low solubility in water, which makes it very easily recovered in commercial processes, a combination of properties that makes it a useful organic reagent.

  5. Non-nucleophilic base - Wikipedia

    en.wikipedia.org/wiki/Non-nucleophilic_base

    As the name suggests, a non-nucleophilic base is a sterically hindered organic base that is a poor nucleophile.Normal bases are also nucleophiles, but often chemists seek the proton-removing ability of a base without any other functions.

  6. 2-tert-Butyl-1,1,3,3-tetramethylguanidine - Wikipedia

    en.wikipedia.org/wiki/2-tert-Butyl-1,1,3,3-tetra...

    2-tert-Butyl-1,1,3,3-tetramethylguanidine is an organic base, also known as Barton's base.It is named after Nobel Prize-winning British chemist Derek Barton.Barton and his assistants prepared a series of guanidines with steric hindrance in 1982; in this case five alkyl groups: four methyl groups and one tert-butyl group.

  7. Base (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Base_(chemistry)

    A strong base is a basic chemical compound that can remove a proton (H +) from (or deprotonate) a molecule of even a very weak acid (such as water) in an acid–base reaction. Common examples of strong bases include hydroxides of alkali metals and alkaline earth metals, like NaOH and Ca(OH) 2, respectively. Due to their low solubility, some ...

  8. Superbase - Wikipedia

    en.wikipedia.org/wiki/Superbase

    Organic superbases are mostly charge-neutral, nitrogen containing species, where nitrogen act as a proton acceptor. These include the phosphazenes, phosphanes , amidines, and guanidines. Other organic compounds that meet the physicochemical or structural definitions of 'superbase' include proton chelators like the aromatic proton sponges and ...

  9. Category:Non-nucleophilic bases - Wikipedia

    en.wikipedia.org/.../Category:Non-nucleophilic_bases

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