30 relations: Alcohol, Autoxidation, Borate, Coordination complex, Dimethylphosphite, Ester, Journal of Organic Chemistry, Lewis acids and bases, Ligand cone angle, Methanol, Michaelis–Arbuzov reaction, Organic peroxide, Organophosphate, Orthoester, Perkow reaction, Phosphinite, Phosphonate, Phosphonite, Phosphorous acid, Phosphorus trichloride, Polyvinyl chloride, Reducing agent, Stabilizer (chemistry), Tautomer, Transesterification, Triethylphosphite, Trimethyl phosphite, Trimethylolpropane phosphite, Triphenyl phosphite, Wender Taxol total synthesis.
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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Autoxidation
Autoxidation is any oxidation that occurs in open air or in presence of oxygen (and sometimes UV radiation) and forms peroxides and hydroperoxides.
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Borate
Borates are the name for a large number of boron-containing oxyanions.
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Coordination complex
In chemistry, a coordination complex consists of a central atom or ion, which is usually metallic and is called the coordination centre, and a surrounding array of bound molecules or ions, that are in turn known as ligands or complexing agents.
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Dimethylphosphite
Dimethylphosphite is an organophosphorus compound with the formula (CH3O)2P(O)H.
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Ester
In chemistry, an ester is a chemical compound derived from an acid (organic or inorganic) in which at least one –OH (hydroxyl) group is replaced by an –O–alkyl (alkoxy) group.
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Journal of Organic Chemistry
The Journal of Organic Chemistry, colloquially known as JOC or J Org, is a peer-reviewed scientific journal for original contributions of fundamental research in all branches of theory and practice in organic and bioorganic chemistry.
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Lewis acids and bases
A Lewis acid is a chemical species that contains an empty orbital which is capable of accepting an electron pair from a Lewis base to form a Lewis adduct.
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Ligand cone angle
thumb The ligand cone angle (a common example being the Tolman cone angle or θ) is a measure of the size of a ligand.
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Methanol
Methanol, also known as methyl alcohol among others, is a chemical with the formula CH3OH (a methyl group linked to a hydroxyl group, often abbreviated MeOH).
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Michaelis–Arbuzov reaction
The Michaelis–Arbuzov reaction (also called the Arbuzov reaction) is the chemical reaction of a trialkyl phosphite and an alkyl halide to form a phosphonate.
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Organic peroxide
Organic peroxides are organic compounds containing the peroxide functional group (ROOR′).
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Organophosphate
Organophosphates (also known as phosphate esters) are a class of organophosphorus compounds with the general structure O.
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Orthoester
In organic chemistry, an orthoester is a functional group containing three alkoxy groups attached to one carbon atom, i.e. with the general formula RC(OR′)3.
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Perkow reaction
The Perkow reaction is an organic reaction in which a trialkyl phosphite ester reacts with a haloketone to form a dialkyl vinyl phosphate and an alkyl halide.
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Phosphinite
Phosphinites are organophosphorus compounds with the formula P(OR)R2.
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Phosphonate
Phosphonates and phosphonic acids are organophosphorus compounds containing C−PO(OH)2 or C−PO(OR)2 groups (where R.
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Phosphonite
Phosphonites are organophosphorus compounds with the formula P(OR)2R.
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Phosphorous acid
Phosphorous acid is the compound described by the formula H3PO3.
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Phosphorus trichloride
Phosphorus trichloride is a chemical compound of phosphorus and chlorine, having the chemical formula PCl3.
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Polyvinyl chloride
Polyvinyl chloride, also known as polyvinyl or '''vinyl''', commonly abbreviated PVC, is the world's third-most widely produced synthetic plastic polymer, after polyethylene and polypropylene.
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Reducing agent
A reducing agent (also called a reductant or reducer) is an element (such as calcium) or compound that loses (or "donates") an electron to another chemical species in a redox chemical reaction.
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Stabilizer (chemistry)
In industrial chemistry, a stabilizer is a chemical that is used to prevent degradation.
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Tautomer
Tautomers are constitutional isomers of organic compounds that readily interconvert.
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Transesterification
In organic chemistry, transesterfication is the process of exchanging the organic group R″ of an ester with the organic group R′ of an alcohol.
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Triethylphosphite
Triethylphosphite is an organophosphorus compound with the formula P(OCH2CH3)3, often abbreviated P(OEt)3.
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Trimethyl phosphite
Trimethylphosphite is an organophosphorus compound with the formula P(OCH3)3, often abbreviated P(OMe)3.
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Trimethylolpropane phosphite
Trimethylolpropane phosphite, C2H5C(CH2O)3P, is a phosphite ester used as a ligand in organometallic chemistry.
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Triphenyl phosphite
Triphenyl phosphite is the chemical compound with the formula P(OC6H5)3.
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Wender Taxol total synthesis
The Wender Taxol total synthesis in organic chemistry describes a Taxol total synthesis (one of six to date) by the group of Paul Wender at Stanford University published in 1997.
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Dialkyl phosphite, Organophosphite, Phosphite.
References
[1] https://en.wikipedia.org/wiki/Phosphite_ester