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  2. Triphenyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Triphenyl_phosphate

    Triphenyl phosphate (TPhP) is the chemical compound with the formula OP(OC 6 H 5) 3. It is the simplest aromatic organophosphate. This colourless solid is the ester (triester) of phosphoric acid and phenol. It is used as a plasticizer and a fire retardant in a wide variety of settings and products. [3]

  3. Triphenylphosphine oxide - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine_oxide

    Triphenylphosphine oxide (often abbreviated TPPO) is the organophosphorus compound with the formula OP(C 6 H 5) 3, also written as Ph 3 PO or PPh 3 O (Ph = C 6 H 5).It is one of the more common phosphine oxides.

  4. Triphenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Triphenylphosphine

    Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C 6 H 5) 3 and often abbreviated to P Ph 3 or Ph 3 P. It is versatile compound that is widely used as a reagent in organic synthesis and as a ligand for transition metal complexes, including ones that serve as catalysts in organometallic chemistry.

  5. Triphenyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Triphenyl_phosphite

    Triphenylphosphite is a notable example of polyamorphism in organic compounds, namely it exists in two different amorphous forms at temperatures about 200 K. [5] One polymorphic modification of triphenyl phosphite was obtained by means of crystallization in ionic liquids. [6]

  6. Human iron metabolism - Wikipedia

    en.wikipedia.org/wiki/Human_iron_metabolism

    The body regulates iron levels by regulating each of these steps. For instance, enterocytes synthesize more Dcytb, DMT1 and ferroportin in response to iron deficiency anemia. [13] Iron absorption from diet is enhanced in the presence of vitamin C and diminished by excess calcium, zinc, or manganese. [14]

  7. Methylenetriphenylphosphorane - Wikipedia

    en.wikipedia.org/wiki/Methylenetriphenylphosphorane

    Potassium tert-butoxide has been used in place of butyl lithium. [3] Sodium amide has also been used a base. [4] Methylenetriphenylphosphorane is used to replace oxygen centres in aldehydes and ketones with a methylene group, i.e., a methylenation: R 2 CO + Ph 3 PCH 2 → R 2 C=CH 2 + Ph 3 PO. The phosphorus-containing product is ...

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