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2. Phosphite ester - Wikipedia

   en.wikipedia.org/wiki/Phosphite_ester

   Phosphite esters may be used as reducing agents in more specialised cases. For example, triethylphosphite is known to reduce certain hydroperoxides to alcohols formed by autoxidation [7] (scheme). In this process the phosphite is converted to a phosphate ester. This reaction type is also utilized in the Wender Taxol total synthesis.

3. Tris(2,4-di-tert-butylphenyl)phosphite - Wikipedia

   en.wikipedia.org/wiki/Tris(2,4-di-tert-butyl...

   It also reduces discoloration (yellowing) of plastics. The compound is a phosphite ester formed by the reaction of 2,4-di-tert-butylphenol with phosphorus trichloride. [1] It is an approved food contact materials in the US. [2]

4. Organophosphate - Wikipedia

   en.wikipedia.org/wiki/Organophosphate

   Esterifications of phosphoric acid with alcohols proceed less readily than the more common carboxylic acid esterifications, with the reactions rarely proceeding much further than the phosphate mono-ester. The reaction requires high temperatures, under which the phosphoric acid can dehydrate to form poly-phosphoric acids.

5. Organophosphorus chemistry - Wikipedia

   en.wikipedia.org/wiki/Organophosphorus_chemistry

   Organophosphorus chemistry is the scientific study of the synthesis and properties of organophosphorus compounds, which are organic compounds containing phosphorus. [1] They are used primarily in pest control as an alternative to chlorinated hydrocarbons that persist in the environment.

6. Trimethyl phosphite - Wikipedia

   en.wikipedia.org/wiki/Trimethyl_phosphite

   Trimethyl phosphite is an organophosphorus compound with the formula P(OCH 3) 3, often abbreviated P(OMe) 3.It is a colorless liquid with a highly pungent odor. It is the simplest phosphite ester and finds used as a ligand in organometallic chemistry and as a reagent in organic synthesis.

7. Triethyl phosphite - Wikipedia

   en.wikipedia.org/wiki/Triethyl_phosphite

   Triethyl phosphite (TEP) is an organophosphorus compound, specifically a phosphite ester, with the formula P(OCH 2 CH 3) 3, often abbreviated P(OEt) 3. It is a colorless, malodorous liquid. It is used as a ligand in organometallic chemistry and as a reagent in organic synthesis.

8. Phosphonate - Wikipedia

   en.wikipedia.org/wiki/Phosphonate

   General ester of phosphonic acid; in fact, the phosphorus has a formal charge of +1, the oxygen above it has a formal charge of −1, and the bond between them is single. In organic chemistry, phosphonates or phosphonic acids are organophosphorus compounds containing C−PO(OR) 2 groups, where R is an organic group (alkyl, aryl).

9. Phosphite (ion) - Wikipedia

   en.wikipedia.org/wiki/Phosphite_(ion)

   The situation is confusing because of the similarity in name between phosphite and phosphate (a major plant nutrient and fertilizer ingredient), and controversial because phosphites have sometimes been advertised as fertilizers, even though they are converted to phosphate too slowly to serve as a plant's main phosphorus source.