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  2. Non-nucleophilic base - Wikipedia

    en.wikipedia.org/wiki/Non-nucleophilic_base

    Download QR code; Print/export Download as PDF; ... As the name suggests, a non-nucleophilic base is a sterically hindered organic base that is a poor nucleophile ...

  3. Category:Non-nucleophilic bases - Wikipedia

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

    Download QR code; Print/export ... Pages in category "Non-nucleophilic bases" ... This list may not reflect recent changes. Non-nucleophilic base; B. 1,8-Bis ...

  4. Lithium tetramethylpiperidide - Wikipedia

    en.wikipedia.org/wiki/Lithium_tetramethylpiperidide

    Download as PDF; Printable version; In other projects ... It is used as a non-nucleophilic base, being comparable to LiHMDS in terms of steric hindrance. Synthesis

  5. 2,2,6,6-Tetramethylpiperidine - Wikipedia

    en.wikipedia.org/wiki/2,2,6,6-tetramethylpiperidine

    TMP is the starting material for an even stronger base, lithium tetramethylpiperidide and the radical species TEMPO. Another non-nucleophilic base is N,N-diisopropylethylamine . Its aqueous p K aH (conjugate acid dissociation constant, a measure of basicity) is 11.07 at 25 °C, [ 1 ] while its p K a (acid dissociation constant, a measure of ...

  6. 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.

  7. 1,1,3,3-Tetramethylguanidine - Wikipedia

    en.wikipedia.org/wiki/1,1,3,3-Tetramethylguanidine

    Tetramethylguanidine is mainly used as a strong, non-nucleophilic base for alkylations, often as a substitute for the more expensive DBU and DBN. [3] Since it is highly water-soluble, it is easily removed from mixtures in organic solvents. It is also used as a base-catalyst in the production of polyurethane. [4]

  8. 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.

  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)