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- 2,3-sigmatropic_rearrangement abstract "2,3-Sigmatropic rearrangements are a type of sigmatropic rearrangements and can be classified into two types. Rearrangements of allylic sulfoxides, amine oxides, selenoxides are neutral. Rearrangements of carbanions of allyl ethers are anionic. The general scheme for this kind of rearrangement is:Atom Y may be sulfur, selenium, or nitrogen. If Y is nitrogen, the reaction is referred to as the Sommelet–Hauser rearrangement; if Y is oxygen, then it is called a 2,3-Wittig rearrangement (not to be confused with the well-known Wittig reaction, which involves a phosphonium ylide). If Y is sulphur, the product can be treated with a thiophile to generate an allylic alcohol in what is known as the Mislow–Evans rearrangement.A [2,3]-rearrangement may result in carbon-carbon bond formation. It can also be used as a ring-expansion reaction.".
- 2,3-sigmatropic_rearrangement thumbnail 2,3-sigmatropic_rearrangement.svg?width=300.
- 2,3-sigmatropic_rearrangement wikiPageID "3281044".
- 2,3-sigmatropic_rearrangement wikiPageLength "2458".
- 2,3-sigmatropic_rearrangement wikiPageOutDegree "37".
- 2,3-sigmatropic_rearrangement wikiPageRevisionID "551457257".
- 2,3-sigmatropic_rearrangement wikiPageWikiLink 2,3-Wittig_rearrangement.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Alcohol.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Alkene.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Allyl.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Aryl.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Carbanion.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Category:Reaction_mechanisms.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Cis–trans_isomerism.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Diastereomer.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Double_bond.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Endo-exo_isomerism.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Ether.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Ion.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Mislow–Evans_rearrangement.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Nitrogen.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Organoselenium_chemistry.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Oxide.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink PH.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Ring_expansion_and_ring_contraction.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Selenium.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Sigmatropic_reaction.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Sommelet–Hauser_rearrangement.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Stereochemistry.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Stereoselectivity.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Sulfoxide.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Sulfur.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Syn_and_anti_addition.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Transition_state.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Wittig_reaction.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink Ylide.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink File:2,3-sigmatropic_rearrangement.svg.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink File:23stereochem.png.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink File:Ringenlarge.png.
- 2,3-sigmatropic_rearrangement wikiPageWikiLink File:Sulfoxide_rearrangement.svg.
- 2,3-sigmatropic_rearrangement wikiPageWikiLinkText "2,3-sigmatropic rearrangement".
- 2,3-sigmatropic_rearrangement wikiPageUsesTemplate Template:Reflist.
- 2,3-sigmatropic_rearrangement subject Category:Reaction_mechanisms.
- 2,3-sigmatropic_rearrangement subject Category:Rearrangement_reactions.
- 2,3-sigmatropic_rearrangement type Reaction.
- 2,3-sigmatropic_rearrangement comment "2,3-Sigmatropic rearrangements are a type of sigmatropic rearrangements and can be classified into two types. Rearrangements of allylic sulfoxides, amine oxides, selenoxides are neutral. Rearrangements of carbanions of allyl ethers are anionic. The general scheme for this kind of rearrangement is:Atom Y may be sulfur, selenium, or nitrogen.".
- 2,3-sigmatropic_rearrangement label "2,3-sigmatropic rearrangement".
- 2,3-sigmatropic_rearrangement sameAs Q4596771.
- 2,3-sigmatropic_rearrangement sameAs Rearreglo_sigmatrópico_2,3.
- 2,3-sigmatropic_rearrangement sameAs Réarrangement_sigmatropique_2,3.
- 2,3-sigmatropic_rearrangement sameAs m.093298.
- 2,3-sigmatropic_rearrangement sameAs Q4596771.
- 2,3-sigmatropic_rearrangement wasDerivedFrom 2,3-sigmatropic_rearrangement?oldid=551457257.
- 2,3-sigmatropic_rearrangement depiction 2,3-sigmatropic_rearrangement.svg.
- 2,3-sigmatropic_rearrangement isPrimaryTopicOf 2,3-sigmatropic_rearrangement.