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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. 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.

4. Category:Phosphorus(III) compounds - Wikipedia

   en.wikipedia.org/wiki/Category:Phosphorus(III...

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5. Category:Organophosphites - Wikipedia

   en.wikipedia.org/wiki/Category:Organophosphites

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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. Organophosphorus chemistry - Wikipedia

   en.wikipedia.org/wiki/Organophosphorus_chemistry

   Phosphites, sometimes called phosphite esters, have the general structure P(OR) 3 with oxidation state +3. Such species arise from the alcoholysis of phosphorus trichloride: PCl 3 + 3 ROH → P(OR) 3 + 3 HCl. The reaction is general, thus a vast number of such species are known.

8. Trimethylolpropane phosphite - Wikipedia

   en.wikipedia.org/wiki/Trimethylolpropane_phosphite

   Trimethylolpropane phosphite, C 2 H 5 C(CH 2 O) 3 P, is a phosphite ester used as a ligand in organometallic chemistry. Trimethylolpropane phosphite is sometimes abbreviated to EtCage. It is a white solid that is soluble in organic solvents. It is also highly toxic. [1]

9. Phosphite - Wikipedia

   en.wikipedia.org/?title=Phosphite&redirect=no

   This page was last edited on 13 July 2017, at 14:09 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may ...