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.
New!!: Triphenylphosphine oxide and Alcohol · See more »
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.
New!!: Triphenylphosphine oxide and Crystallization · See more »
HSAB theory
HSAB concept is an initialism for "hard and soft (Lewis) acids and bases".
New!!: Triphenylphosphine oxide and HSAB theory · See more »
Inorganic Chemistry (journal)
Inorganic Chemistry is a biweekly peer-reviewed scientific journal published by the American Chemical Society since 1962.
New!!: Triphenylphosphine oxide and Inorganic Chemistry (journal) · See more »
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.
New!!: Triphenylphosphine oxide and Journal of the American Chemical Society · See more »
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).
New!!: Triphenylphosphine oxide and Mitsunobu reaction · See more »
Organic synthesis
Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.
New!!: Triphenylphosphine oxide and Organic synthesis · See more »
Organophosphorus compound
Organophosphorus compounds are organic compounds containing phosphorus.
New!!: Triphenylphosphine oxide and Organophosphorus compound · See more »
Phenol
Phenol, also known as phenolic acid, is an aromatic organic compound with the molecular formula C6H5OH.
New!!: Triphenylphosphine oxide and Phenol · See more »
Phenyl group
In organic chemistry, the phenyl group or phenyl ring is a cyclic group of atoms with the formula C6H5.
New!!: Triphenylphosphine oxide and Phenyl group · See more »
Phosphorus pentachloride
Phosphorus pentachloride is the chemical compound with the formula PCl5.
New!!: Triphenylphosphine oxide and Phosphorus pentachloride · See more »
Phosphoryl chloride
Phosphoryl chloride (commonly called phosphorus oxychloride) is a colourless liquid with the formula 3.
New!!: Triphenylphosphine oxide and Phosphoryl chloride · See more »
Staudinger reaction
The Staudinger reaction is a chemical reaction of an azide with a phosphine or phosphite produces an iminophosphorane.
New!!: Triphenylphosphine oxide and Staudinger reaction · See more »
Trichlorosilane
Trichlorosilane is an inorganic compound with the formula HSiCl3.
New!!: Triphenylphosphine oxide and Trichlorosilane · See more »
Triphenylphosphine
Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C6H5)3 - often abbreviated to PPh3 or Ph3P.
New!!: Triphenylphosphine oxide and Triphenylphosphine · See more »
Triphenylphosphine sulfide
Triphenylphosphine sulfide (IUPAC name: triphenyl-λ5-phosphanethione) is the organophosphorus compound with the formula (C6H5)3PS, usually written Ph3PS (where Ph.
New!!: Triphenylphosphine oxide and Triphenylphosphine sulfide · See more »
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.
New!!: Triphenylphosphine oxide and Wittig reaction · See more »