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- Stevens_rearrangement abstract "The Stevens rearrangement in organic chemistry is an organic reaction converting quaternary ammonium salts and sulfonium salts to the corresponding amines or sulfides in presence of a strong base in a 1,2-rearrangement.The reactants can be obtained by alkylation of the corresponding amines and sulfides. The substituent R next the amine methylene bridge is an electron-withdrawing group.The original 1928 publication by Thomas S. Stevens concerned the reaction of 1-phenyl-2- (N, N-dimethyl) ethanone with benzyl bromide to the ammonium salt followed by the rearrangement reaction with sodium hydroxide in water to the rearranged amine.A 1932 publication described the corresponding sulfur reaction.".
- Stevens_rearrangement thumbnail Stevens_rearrangement_overview.svg?width=300.
- Stevens_rearrangement wikiPageID "5658880".
- Stevens_rearrangement wikiPageLength "6867".
- Stevens_rearrangement wikiPageOutDegree "44".
- Stevens_rearrangement wikiPageRevisionID "705703242".
- Stevens_rearrangement wikiPageWikiLink 1,2-rearrangement.
- Stevens_rearrangement wikiPageWikiLink Alkylation.
- Stevens_rearrangement wikiPageWikiLink Amine.
- Stevens_rearrangement wikiPageWikiLink Antarafacial_and_suprafacial.
- Stevens_rearrangement wikiPageWikiLink Base_(chemistry).
- Stevens_rearrangement wikiPageWikiLink Benzyl_bromide.
- Stevens_rearrangement wikiPageWikiLink Cage_effect.
- Stevens_rearrangement wikiPageWikiLink Carbon–carbon_bond.
- Stevens_rearrangement wikiPageWikiLink Carnitine_biosynthesis.
- Stevens_rearrangement wikiPageWikiLink Catalysis.
- Stevens_rearrangement wikiPageWikiLink Category:Name_reactions.
- Stevens_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- Stevens_rearrangement wikiPageWikiLink Concerted_reaction.
- Stevens_rearrangement wikiPageWikiLink Cyclophane.
- Stevens_rearrangement wikiPageWikiLink Deprotonation.
- Stevens_rearrangement wikiPageWikiLink Diazo.
- Stevens_rearrangement wikiPageWikiLink Enzyme.
- Stevens_rearrangement wikiPageWikiLink Gamma-butyrobetaine_dioxygenase.
- Stevens_rearrangement wikiPageWikiLink Hofmann_elimination.
- Stevens_rearrangement wikiPageWikiLink Homolysis_(chemistry).
- Stevens_rearrangement wikiPageWikiLink In_situ.
- Stevens_rearrangement wikiPageWikiLink Meldonium.
- Stevens_rearrangement wikiPageWikiLink Methylene_bridge.
- Stevens_rearrangement wikiPageWikiLink Organic_chemistry.
- Stevens_rearrangement wikiPageWikiLink Organic_reaction.
- Stevens_rearrangement wikiPageWikiLink Polar_effect.
- Stevens_rearrangement wikiPageWikiLink Quaternary_ammonium_cation.
- Stevens_rearrangement wikiPageWikiLink Reaction_mechanism.
- Stevens_rearrangement wikiPageWikiLink Reflux.
- Stevens_rearrangement wikiPageWikiLink Sodium_hydroxide.
- Stevens_rearrangement wikiPageWikiLink Sommelet–Hauser_rearrangement.
- Stevens_rearrangement wikiPageWikiLink Substituent.
- Stevens_rearrangement wikiPageWikiLink Sulfide.
- Stevens_rearrangement wikiPageWikiLink Sulfonium.
- Stevens_rearrangement wikiPageWikiLink Walden_inversion.
- Stevens_rearrangement wikiPageWikiLink Xylene.
- Stevens_rearrangement wikiPageWikiLink Ylide.
- Stevens_rearrangement wikiPageWikiLink File:Stevens1928rearrangement.png.
- Stevens_rearrangement wikiPageWikiLink File:Stevens_mechanism.png.
- Stevens_rearrangement wikiPageWikiLink File:Stevens_rearrangement_applied.png.
- Stevens_rearrangement wikiPageWikiLink File:Stevens_rearrangement_overview.svg.
- Stevens_rearrangement wikiPageWikiLinkText "Steven's type rearrangement".
- Stevens_rearrangement wikiPageWikiLinkText "Stevens rearrangement".
- Stevens_rearrangement wikiPageWikiLinkText "Stevens-like rearrangement".
- Stevens_rearrangement wikiPageUsesTemplate Template:Distinguish.
- Stevens_rearrangement wikiPageUsesTemplate Template:Reflist.
- Stevens_rearrangement wikiPageUsesTemplate Template:Use_dmy_dates.
- Stevens_rearrangement subject Category:Name_reactions.
- Stevens_rearrangement subject Category:Rearrangement_reactions.
- Stevens_rearrangement hypernym Reaction.
- Stevens_rearrangement type Disease.
- Stevens_rearrangement type Eponym.
- Stevens_rearrangement type Reaction.
- Stevens_rearrangement type Thing.
- Stevens_rearrangement comment "The Stevens rearrangement in organic chemistry is an organic reaction converting quaternary ammonium salts and sulfonium salts to the corresponding amines or sulfides in presence of a strong base in a 1,2-rearrangement.The reactants can be obtained by alkylation of the corresponding amines and sulfides. The substituent R next the amine methylene bridge is an electron-withdrawing group.The original 1928 publication by Thomas S.".
- Stevens_rearrangement label "Stevens rearrangement".
- Stevens_rearrangement differentFrom Stephen_aldehyde_synthesis.
- Stevens_rearrangement sameAs Q906103.
- Stevens_rearrangement sameAs Stevens-Umlagerung.
- Stevens_rearrangement sameAs m.0dyq7_.
- Stevens_rearrangement sameAs Q906103.
- Stevens_rearrangement sameAs 斯蒂文斯重排反应.
- Stevens_rearrangement wasDerivedFrom Stevens_rearrangement?oldid=705703242.
- Stevens_rearrangement depiction Stevens_rearrangement_overview.svg.
- Stevens_rearrangement isPrimaryTopicOf Stevens_rearrangement.