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Summary Of: Wittig reaction

The Wittig reaction was discovered in 1954 by... of the Wittig reaction can be performed... The Wittig reaction has become a popular method for... the Wittig reaction forms the double bond in one position with no ambiguity... The major limitation of the traditional Wittig reaction is that the reaction goes mainly via the... the Wittig reaction has become a standard tool for synthetic organic chemists... The most popular use of the Wittig reaction is for the introduction of a... The second Wittig reaction uses a non... Modification of the Wittig reaction to permit the stereospecific synthesis of certain trisubstituted olefins...

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chemical reaction | aldehyde | ketone | alkene | triphenylphosphine oxide | Wittig Reaction | Georg Wittig | Nobel Prize in Chemistry | organic synthesis | Wittig rearrangement | ylides | Z-alkene | ylide | nucleophilic addition | betaine | triphenylphosphine oxide | aldehydes | ketones | rate-determining step | E-isomer | sterically hindered ketones | The mechanism of the Wittig reaction | reaction mechanism | NMR spectroscopy | cycloaddition | stereochemistry | equilibrate | Maryanoff | Lithium | The mechanism of the Wittig reaction | aliphatic | aromatic | aldehydes | aromatic | aliphatic | unbranched | kinetic reaction control | phosphonium salt | triphenylphosphine | alkyl halide | diethyl ether | THF | phenyllithium | n-butyllithium | C4H9Li | C4H10 | alkyl halide | R-CH2-X | deprotonated | carbanion | Ph | Horner-Wadsworth-Emmons | alkoxides | sodium hydroxide | | octet | hypervalency | alkenes | imines | nucleophilic | alkene | elimination | dehydrohalogenation | alkyl halides | regioisomers | Zaitsev's rule | ketones | aldehydes | carboxylic acid | esters | carbonyl | OH | OR | nitro | sterically hindered | Horner-Wadsworth-Emmons (HWE) reaction | aldehydes | in situ | alcohol | alkyl halide | aromatic rings | ethers | ester | nitrile | conjugated | stereochemistry | Z-isomer | DMF | LiI | NaI | The Schlosser variant of the Wittig reaction | erythro | betaine | Z-alkene | threo | phenyllithium | HCl | E-alkene | E. J. Corey | stereoselective | allylic alcohols | An example of the Schlosser variant of the Wittig reaction | Two examples of the Wittig reaction using methylenetriphenylphosphorane | methylene | camphor | potassium tert-butoxide | sodium amide | aldehyde | THF | nitro | azo | phenoxide | polymer | UV radiation | leukotriene A | epoxide | ester | An example of the use of the Wittig reaction in synthesis, making Leukotriene A methyl ester | Methoxymethylenetriphenylphosphine | Corey-Chaykovsky reagent | Horner-Wadsworth-Emmons reaction | Julia-Lythgoe olefination | Peterson olefination | Tebbe reagent | Organophosphorus chemistry | Homologation reaction | Georg Wittig | Ulrich Schöllkopf | Chemische Berichte | doi | Chemische Berichte | doi | ISBN 0-521-31117-9 | Angewandte Chemie International Edition | doi | J. Am. Chem. Soc. | doi | B. E. Maryanoff | B. E. Maryanoff | B. E. Maryanoff | B. E. Maryanoff | J. Am. Chem. Soc. | doi | J. Am. Chem. Soc. | doi | Org. Synth. | Angew. Chem. | doi | Angewandte Chemie International Edition in English | doi | E. J. Corey | J. Am. Chem. Soc. | doi | Chem. Rev. | doi | doi | Tetrahedron Letters | doi | J. Am. Chem. Soc. | doi | Organic Syntheses | Organic Syntheses | Categories | Carbon-carbon bond forming reactions | Name reactions |
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