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  2. Non-nucleophilic base - Wikipedia

    en.wikipedia.org/wiki/Non-nucleophilic_base

    Lithium tetramethylpiperidide (LiTMP or harpoon base) Other strong non-nucleophilic bases are sodium hydride and potassium hydride. These compounds are dense, salt-like materials that are insoluble and operate by surface reactions. Some reagents are of high basicity (pK a of conjugate acid around 17) but of modest but not negligible ...

  3. Category:Non-nucleophilic bases - Wikipedia

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

    Pages in category "Non-nucleophilic bases" The following 26 pages are in this category, out of 26 total. This list may not reflect recent changes. ...

  4. 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. [1]

  5. N,N-Diisopropylethylamine - Wikipedia

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

    N,N-Diisopropylethylamine, or Hünig's base, is an organic compound that is a tertiary amine. It is named after the German chemist Siegfried Hünig . It is used in organic chemistry as a non-nucleophilic base. It is commonly abbreviated as DIPEA, DIEA, or i-Pr 2 NEt.

  6. Potassium bis(trimethylsilyl)amide - Wikipedia

    en.wikipedia.org/wiki/Potassium_bis...

    It is a strong, non-nucleophilic base with an approximate pK a of 26 (compare to lithium diisopropylamide, at 36). [citation needed] Structure.

  7. Lithium bis(trimethylsilyl)amide - Wikipedia

    en.wikipedia.org/wiki/Lithium_bis(trimethylsilyl...

    LiHMDS is often used in organic chemistry as a strong non-nucleophilic base. [3] Its conjugate acid has a pK a of ~26, [4] making it is less basic than other lithium bases, such as LDA (pK a of conjugate acid ~36). It is relatively more sterically hindered and hence less nucleophilic than other lithium bases.

  8. Phosphazene - Wikipedia

    en.wikipedia.org/wiki/Phosphazene

    BEMP and P4-t-Bu|t-Bu-P 4 have attracted attention because they are low-nucleophilic, which precludes their participating in competing reactions. Being non-ionic ("charge-neutral"), they are soluble in nonpolar solvents. Protonation takes place at a doubly bonded nitrogen atom. [3]

  9. 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 ...