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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. 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.

  5. 1,8-Diazabicyclo(5.4.0)undec-7-ene - Wikipedia

    en.wikipedia.org/wiki/1,8-Diazabicyclo(5.4.0...

    As a reagent in organic chemistry, DBU is used as a ligand and base. As a base, protonation occurs at the imine nitrogen. [5] Lewis acids also attach to the same nitrogen. [6] These properties recommend DBU for use as a catalyst, for example as a curing agent for epoxy resins and polyurethane.

  6. 1,5-Diazabicyclo (4.3.0)non-5-ene - Wikipedia

    en.wikipedia.org/wiki/1,5-Diazabicyclo(4.3.0)non...

    1,5-Diazabicyclo[4.3.0]non-5-ene (DBN) is a chemical compound with the formula C 7 H 12 N 2. [1] It is an amidine base used in organic synthesis. A related compound with related functions is 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). The relatively complex nature of the formal names for DBU and DBN (hence the common use of acronyms) reflects the ...

  7. Phosphazene - Wikipedia

    en.wikipedia.org/wiki/Phosphazene

    Phosphazene bases are strong non-metallic non-ionic and low-nucleophilic bases. They are stronger bases than regular amine or amidine bases. Protonation takes place at a doubly bonded nitrogen atom. Related to phosphazene bases are the Verkade bases, which feature P(III) with three amido substituents and a transannular amine.

  8. Category:Bases (chemistry) - Wikipedia

    en.wikipedia.org/wiki/Category:Bases_(chemistry)

    Bases are defined by the Brønsted–Lowry theory as chemical substances that can accept a proton, i.e., a hydrogen ion. In water this is equivalent to a hydronium ion). The Lewis theory instead defines a Base as an electron-pair donor. The Lewis definition is broader — all Brønsted–Lowry bases are also Lewis bases.

  9. Lithium tetramethylpiperidide - Wikipedia

    en.wikipedia.org/wiki/Lithium_tetramethylpiperidide

    CAS Number. 38227-87-1 ... It is used as a non-nucleophilic base, being comparable to LiHMDS in terms of steric hindrance. Synthesis