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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. Diphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphine

    In the laboratory, diphenylphosphine is a common intermediate. It can be deprotonated to give diphenylphosphide derivatives: [2] Ph 2 PH + n BuLi → Ph 2 PLi + n BuH. The preparation of phosphine ligands, Wittig-Horner reagents, and phosphonium salts are commonly accomplished by alkylating diphenylphosphine.

  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. 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.

  7. 1,2-Bis (diphenylphosphino)ethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Bis(diphenylphosphino...

    Printable version; In other projects Wikimedia Commons; Wikidata item; Appearance. move to sidebar hide. 1,2-Bis(diphenylphosphino)ethane ... CAS Number. 1663-45-2 ...

  8. Diphenylphosphine oxide - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphine_oxide

    Diphenylphosphine oxide exists in equilibrium with its minor tautomer diphenylphosphinous acid, ((C 6 H 5) 2 POH: (C 6 H 5) 2 P(O)H ⇌ (C 6 H 5) 2 POH. Diphenylphosphine oxide is used in Buchwald-Hartwig coupling reactions to introduce diphenylphosphino substituents.

  9. DPEphos - Wikipedia

    en.wikipedia.org/wiki/DPEphos

    Bis[(2-diphenylphosphino)phenyl] ether, also known as DPEphos, is a wide bite angle diphosphine ligand used in inorganic and organometallic chemistry.The name DPEphos is derived from diphenyl ether (DPE) which makes up the ligand's backbone.