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  2. Diphenylphosphoryl azide - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphoryl_azide

    It is now suggested that this reaction proceeds through the intermediate mixed anhydride, resulting from attack by the nucleophilic carboxylate anion on the phosphorus atom, with expulsion of the azide ion. The latter then attacks the carbonyl carbon atom, to give the acyl azide and loss of the diphenylphosphate anion, known to be a good ...

  3. Organic azide - Wikipedia

    en.wikipedia.org/wiki/Organic_azide

    The azide functional group can be shown by two resonance structures. An organic azide is an organic compound that contains an azide (– N 3) functional group. [1] Because of the hazards associated with their use, few azides are used commercially although they exhibit interesting reactivity for researchers.

  4. Curtius rearrangement - Wikipedia

    en.wikipedia.org/wiki/Curtius_rearrangement

    The acyl azide is usually made from the reaction of acid chlorides or anhydrides [6] with sodium azide [7] or trimethylsilyl azide. [8] Acyl azides are also obtained from treating acylhydrazines with nitrous acid. [9] Alternatively, the acyl azide can be formed by the direct reaction of a carboxylic acid with diphenylphosphoryl azide (DPPA ...

  5. Phenyl azide - Wikipedia

    en.wikipedia.org/wiki/Phenyl_azide

    Phenyl azide is an organic compound with the formula C 6 H 5 N 3. It is one of the prototypical organic azides. It is a pale yellow oily liquid with a pungent odor. The structure consists of a linear azide substituent bound to a phenyl group. The C−N=N angle is approximately 116°.

  6. Azide - Wikipedia

    en.wikipedia.org/wiki/Azide

    In chemistry, azide (/ ˈ eɪ z aɪ d /, AY-zyd) is a linear, polyatomic anion with the formula N − 3 and structure − N=N + =N −.It is the conjugate base of hydrazoic acid HN 3. Organic azides are organic compounds with the formula RN 3, containing the azide functional group. [1]

  7. Diphenylphosphite - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphite

    Diphenyl phosphite is a diorganophosphite with the formula (C 6 H 5 O) 2 P(O)H. The molecule is tetrahedral. It is a colorless viscous liquid. The compounds can be prepared by treating phosphorus trichloride with phenol. Many analogues can be prepared similarly.

  8. Diphenyl-2-pyridylphosphine - Wikipedia

    en.wikipedia.org/wiki/Diphenyl-2-pyridylphosphine

    Diphenyl-2-pyridylphosphine is an organophosphorus compound with the formula P(C 6 H 5) 2 (2-C 5 H 4 N). It is the most widely used mono-pyridylphosphine ligand. [1] Other mono-pyridylphosphines ligands (3-, 4-) are not common in chemical literature; however, tris-pyridylphosphines have been thoroughly investigated as ligands in transition metal complexes used for catalysis.

  9. Diphenylzinc - Wikipedia

    en.wikipedia.org/wiki/Diphenylzinc

    CAS Number. 1078-58-6 ... Solvent-free diphenylzinc exists as dimeric PhZn(μ-Ph) 2 ZnPh molecules in the solid state. [1] The dimeric solid state form of diphenylzinc.