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Wittig rearrangement information


Wittig rearrangement may refer to:

  • 1,2-Wittig rearrangement
  • 2,3-Wittig rearrangement

and 19 Related for: Wittig rearrangement information

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Wittig rearrangement

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Wittig rearrangement may refer to: 1,2-Wittig rearrangement 2,3-Wittig rearrangement This disambiguation page lists articles associated with the title...

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Georg Wittig

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1979. Wittig's contributions also include the preparation of phenyllithium and the discovery of the 1,2-Wittig rearrangement and the 2,3-Wittig rearrangement...

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Wittig

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Agency Susan Wittig Albert (born 1940), American mystery writer Wittich Wittig River 1,2-Wittig rearrangement 2,3-Wittig rearrangement Wittig reaction Witting...

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Outline of organic chemistry

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Overman rearrangement Oxy-Cope rearrangement Pinacol rearrangement 1,2-Wittig rearrangement 2,3-Wittig rearrangement Substitution reaction Electrophilic...

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List of organic reactions

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V W X Y Z See also External links 1,2-Wittig rearrangement 1,3-Dipolar cycloaddition 2,3-Wittig rearrangement Acetalisation Acetoacetic ester condensation...

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Conolidine

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available acetyl-pyridine. Notable reactions include a [2,3]-Still-Wittig rearrangement and a conformationally-controlled intramolecular Mannich cyclization...

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Ylide

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a [2,3]-rearrangement, a homoallylhalide is obtained. The active form of Tebbe's reagent is often considered a titanium ylide. Like the Wittig reagent...

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Monique Wittig

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Monique Wittig (French: [vitig]; 13 July 1935 – 3 January 2003) was a French author, philosopher and feminist theorist who wrote about abolition of the...

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Dyotropic reaction

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equilibration of (R3Si1)R2C-O-Si2R3 to (R3Si2)R2C-O-Si1R3.: 36  The 1,2-Wittig rearrangement can also be considered an example of this reaction type. More dyotropic...

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Sigmatropic reaction

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well-known of the sigmatropic rearrangements are the [3,3] Cope rearrangement, Claisen rearrangement, Carroll rearrangement, and the Fischer indole synthesis...

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Radical clock

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sodium naphthalenide, reaction[clarification needed] of enones, the Wittig rearrangement, reductive elimination reactions of dialkylmercury compounds, dioxirane...

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Brook rearrangement

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In organic chemistry the Brook rearrangement refers to any [1,n] carbon to oxygen silyl migration. The rearrangement was first observed in the late 1950s...

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Organolithium reagent

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alkyllithium or LDA forms an anion α to the oxygen, and can proceed to 2,3-Wittig rearrangement. Addition of donor ligands such as TMEDA and HMPA can increase metalation...

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Organic reaction

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elimination reactions, substitution reactions, pericyclic reactions, rearrangement reactions, photochemical reactions and redox reactions. In organic synthesis...

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IUPAC nomenclature for organic chemical transformations

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inventors, the so-called name reactions, such as Knoevenagel condensation, Wittig reaction, Claisen–Schmidt condensation, Schotten–Baumann reaction, and Diels–Alder...

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Imine

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Aza-Wittig-reaction. Condensation of carbon acids with nitroso compounds. The rearrangement of trityl N-haloamines in the Stieglitz rearrangement. By...

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Alkene

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olefinations. The Wittig reaction is illustrative, but other related methods are known, including the Horner–Wadsworth–Emmons reaction. The Wittig reaction involves...

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Allenes

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metallic sodium or magnesium) in the Skattebøl rearrangement (Doering–LaFlamme allene synthesis) via rearrangement of cyclopropylidene carbenes/carbenoids from...

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Ei mechanism

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mechanism). The Wittig modified Hofmann elimination goes through the same Ei mechanism, but instead of using silver oxide and water as base, the Wittig modification...

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