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- Meyer–Schuster_rearrangement abstract "The Meyer–Schuster rearrangement is the chemical reaction described as an acid-catalyzed rearrangement of secondary and tertiary propargyl alcohols to α,β-unsaturated ketones if the alkyne group is internal and α,β-unsaturated aldehydes if the alkyne group is terminal. Reviews have been published by Swaminathan and Narayan, Vartanyan and Banbanyan, and Engel and Dudley, the last of which describes ways to promote the Meyer–Schuster rearrangement over other reactions available to propargyl alcohols.When catalyzed by base, the reaction is called the Favorskii reaction.".
- Meyer–Schuster_rearrangement thumbnail Meyer-Schuster_Rearrangement_Scheme.png?width=300.
- Meyer–Schuster_rearrangement wikiPageID "8002251".
- Meyer–Schuster_rearrangement wikiPageLength "6904".
- Meyer–Schuster_rearrangement wikiPageOutDegree "40".
- Meyer–Schuster_rearrangement wikiPageRevisionID "674730047".
- Meyer–Schuster_rearrangement wikiPageWikiLink Acetylenic.
- Meyer–Schuster_rearrangement wikiPageWikiLink Acid.
- Meyer–Schuster_rearrangement wikiPageWikiLink Aldehyde.
- Meyer–Schuster_rearrangement wikiPageWikiLink Alkyne.
- Meyer–Schuster_rearrangement wikiPageWikiLink Allene.
- Meyer–Schuster_rearrangement wikiPageWikiLink Cage_effect.
- Meyer–Schuster_rearrangement wikiPageWikiLink Cage_effect_(chemistry).
- Meyer–Schuster_rearrangement wikiPageWikiLink Carbocation.
- Meyer–Schuster_rearrangement wikiPageWikiLink Carbonium_ion.
- Meyer–Schuster_rearrangement wikiPageWikiLink Carbonyl.
- Meyer–Schuster_rearrangement wikiPageWikiLink Catalysis.
- Meyer–Schuster_rearrangement wikiPageWikiLink Category:Name_reactions.
- Meyer–Schuster_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- Meyer–Schuster_rearrangement wikiPageWikiLink Chemical_reaction.
- Meyer–Schuster_rearrangement wikiPageWikiLink Diastereomer.
- Meyer–Schuster_rearrangement wikiPageWikiLink Elimination_reaction.
- Meyer–Schuster_rearrangement wikiPageWikiLink Enyne.
- Meyer–Schuster_rearrangement wikiPageWikiLink Favorskii_reaction.
- Meyer–Schuster_rearrangement wikiPageWikiLink Isoindole.
- Meyer–Schuster_rearrangement wikiPageWikiLink Keto-enol_tautomerism.
- Meyer–Schuster_rearrangement wikiPageWikiLink Ketone.
- Meyer–Schuster_rearrangement wikiPageWikiLink Keto–enol_tautomerism.
- Meyer–Schuster_rearrangement wikiPageWikiLink Lactam.
- Meyer–Schuster_rearrangement wikiPageWikiLink Lewis_acid.
- Meyer–Schuster_rearrangement wikiPageWikiLink Lewis_acids_and_bases.
- Meyer–Schuster_rearrangement wikiPageWikiLink Methyl.
- Meyer–Schuster_rearrangement wikiPageWikiLink Methyl_group.
- Meyer–Schuster_rearrangement wikiPageWikiLink Microwave_chemistry.
- Meyer–Schuster_rearrangement wikiPageWikiLink Paclitaxel.
- Meyer–Schuster_rearrangement wikiPageWikiLink Propargyl_alcohol.
- Meyer–Schuster_rearrangement wikiPageWikiLink Rate-determining_step.
- Meyer–Schuster_rearrangement wikiPageWikiLink Reaction_intermediate.
- Meyer–Schuster_rearrangement wikiPageWikiLink Reaction_mechanism.
- Meyer–Schuster_rearrangement wikiPageWikiLink Rearrangement_reaction.
- Meyer–Schuster_rearrangement wikiPageWikiLink Sigmatropic_reaction.
- Meyer–Schuster_rearrangement wikiPageWikiLink Stereoselectivity.
- Meyer–Schuster_rearrangement wikiPageWikiLink Tautomer.
- Meyer–Schuster_rearrangement wikiPageWikiLink Tautomerization.
- Meyer–Schuster_rearrangement wikiPageWikiLink Thioester.
- Meyer–Schuster_rearrangement wikiPageWikiLink Transition_metal.
- Meyer–Schuster_rearrangement wikiPageWikiLink File:Cadierno-microwave-catalysis.svg.
- Meyer–Schuster_rearrangement wikiPageWikiLink File:Meyer-Schuster_Rearrangement_Scheme.png.
- Meyer–Schuster_rearrangement wikiPageWikiLink File:Meyer-schuster-rearrangement.svg.
- Meyer–Schuster_rearrangement wikiPageWikiLink File:Meyer-schuster-taxol.svg.
- Meyer–Schuster_rearrangement wikiPageWikiLink File:Rupe-rearrangement.svg.
- Meyer–Schuster_rearrangement wikiPageWikiLinkText "Meyer–Schuster rearrangement".
- Meyer–Schuster_rearrangement wikiPageWikiLinkText "Meyer–Schuster rearrangement#Rupe rearrangement".
- Meyer–Schuster_rearrangement hasPhotoCollection Meyer–Schuster_rearrangement.
- Meyer–Schuster_rearrangement wikiPageUsesTemplate Template:Reflist.
- Meyer–Schuster_rearrangement subject Category:Name_reactions.
- Meyer–Schuster_rearrangement subject Category:Rearrangement_reactions.
- Meyer–Schuster_rearrangement comment "The Meyer–Schuster rearrangement is the chemical reaction described as an acid-catalyzed rearrangement of secondary and tertiary propargyl alcohols to α,β-unsaturated ketones if the alkyne group is internal and α,β-unsaturated aldehydes if the alkyne group is terminal.".
- Meyer–Schuster_rearrangement label "Meyer–Schuster rearrangement".
- Meyer–Schuster_rearrangement sameAs Meyer-Schuster-Umlagerung.
- Meyer–Schuster_rearrangement sameAs マイヤー・シュスター転位.
- Meyer–Schuster_rearrangement sameAs Meyer-Schuster-omlegging.
- Meyer–Schuster_rearrangement sameAs Rearranjo_de_Meyer-Schuster.
- Meyer–Schuster_rearrangement sameAs m.026n3wx.
- Meyer–Schuster_rearrangement sameAs Q902668.
- Meyer–Schuster_rearrangement sameAs Q902668.
- Meyer–Schuster_rearrangement sameAs 迈耶-舒斯特重排反应.
- Meyer–Schuster_rearrangement wasDerivedFrom Meyer–Schuster_rearrangement?oldid=674730047.
- Meyer–Schuster_rearrangement depiction Meyer-Schuster_Rearrangement_Scheme.png.
- Meyer–Schuster_rearrangement isPrimaryTopicOf Meyer–Schuster_rearrangement.