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Triphenylphosphine oxide

Index Triphenylphosphine oxide

Triphenylphosphine oxide (often abbreviated TPPO) is the organophosphorus compound with the formula OP(C6H5)3, also written as Ph3PO or PPh3O (Ph. [1]

17 relations: Alcohol, Crystallization, HSAB theory, Inorganic Chemistry (journal), Journal of the American Chemical Society, Mitsunobu reaction, Organic synthesis, Organophosphorus compound, Phenol, Phenyl group, Phosphorus pentachloride, Phosphoryl chloride, Staudinger reaction, Trichlorosilane, Triphenylphosphine, Triphenylphosphine sulfide, Wittig reaction.

Alcohol

In chemistry, an alcohol is any organic compound in which the hydroxyl functional group (–OH) is bound to a carbon.

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Crystallization

Crystallization is the (natural or artificial) process by which a solid forms, where the atoms or molecules are highly organized into a structure known as a crystal.

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HSAB theory

HSAB concept is an initialism for "hard and soft (Lewis) acids and bases".

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Inorganic Chemistry (journal)

Inorganic Chemistry is a biweekly peer-reviewed scientific journal published by the American Chemical Society since 1962.

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Journal of the American Chemical Society

The Journal of the American Chemical Society (also known as JACS) is a weekly peer-reviewed scientific journal that was established in 1879 by the American Chemical Society.

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Mitsunobu reaction

The Mitsunobu reaction is an organic reaction that converts an alcohol into a variety of functional groups, such as an ester, using triphenylphosphine and an azodicarboxylate such as diethyl azodicarboxylate (DEAD) or diisopropyl azodicarboxylate (DIAD).

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Organic synthesis

Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.

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Organophosphorus compound

Organophosphorus compounds are organic compounds containing phosphorus.

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Phenol

Phenol, also known as phenolic acid, is an aromatic organic compound with the molecular formula C6H5OH.

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Phenyl group

In organic chemistry, the phenyl group or phenyl ring is a cyclic group of atoms with the formula C6H5.

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Phosphorus pentachloride

Phosphorus pentachloride is the chemical compound with the formula PCl5.

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Phosphoryl chloride

Phosphoryl chloride (commonly called phosphorus oxychloride) is a colourless liquid with the formula 3.

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Staudinger reaction

The Staudinger reaction is a chemical reaction of an azide with a phosphine or phosphite produces an iminophosphorane.

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Trichlorosilane

Trichlorosilane is an inorganic compound with the formula HSiCl3.

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Triphenylphosphine

Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C6H5)3 - often abbreviated to PPh3 or Ph3P.

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Triphenylphosphine sulfide

Triphenylphosphine sulfide (IUPAC name: triphenyl-λ5-phosphanethione) is the organophosphorus compound with the formula (C6H5)3PS, usually written Ph3PS (where Ph.

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Wittig reaction

The Wittig reaction or Wittig olefination is a chemical reaction of an aldehyde or ketone with a triphenyl phosphonium ylide (often called a Wittig reagent) to give an alkene and triphenylphosphine oxide.

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Redirects here:

OPPh3, PPh3O, Ph3PO, Tppo.

References

[1] https://en.wikipedia.org/wiki/Triphenylphosphine_oxide

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