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- Overman_rearrangement abstract "The Overman rearrangement is a chemical reaction that can be described as a Claisen rearrangement of allylic alcohols to give allylic trichloroacetamides through an imidate intermediate. The Overman rearrangement was discovered in 1974 by Larry Overman.The [3,3]-sigmatropic rearrangement is diastereoselective requires heating but can also be catalyzed by Hg(II), or Pd(II) salts. The resulting allylamine structures can be transformed into many chemically and biologically important natural and un-natural amino acids (like (1-adamantyl)glycine).The Overman rearrangement may also be used for asymmetric synthesis.".
- Overman_rearrangement thumbnail Overman_Rearrangement_scheme.svg?width=300.
- Overman_rearrangement wikiPageID "2655809".
- Overman_rearrangement wikiPageLength "3208".
- Overman_rearrangement wikiPageOutDegree "18".
- Overman_rearrangement wikiPageRevisionID "617785519".
- Overman_rearrangement wikiPageWikiLink Adamantane.
- Overman_rearrangement wikiPageWikiLink Allyl.
- Overman_rearrangement wikiPageWikiLink Carboximidate.
- Overman_rearrangement wikiPageWikiLink Category:Carboximidates.
- Overman_rearrangement wikiPageWikiLink Category:Name_reactions.
- Overman_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- Overman_rearrangement wikiPageWikiLink Chemical_reaction.
- Overman_rearrangement wikiPageWikiLink Claisen_rearrangement.
- Overman_rearrangement wikiPageWikiLink Diastereomer.
- Overman_rearrangement wikiPageWikiLink Enantioselective_synthesis.
- Overman_rearrangement wikiPageWikiLink Journal_of_Organic_Chemistry.
- Overman_rearrangement wikiPageWikiLink Larry_E._Overman.
- Overman_rearrangement wikiPageWikiLink Mercury_(element).
- Overman_rearrangement wikiPageWikiLink Palladium.
- Overman_rearrangement wikiPageWikiLink Pinner_reaction.
- Overman_rearrangement wikiPageWikiLink Sigmatropic_reaction.
- Overman_rearrangement wikiPageWikiLink Tetrahedron_Letters.
- Overman_rearrangement wikiPageWikiLink File:Overman_Rearrangement_scheme.svg.
- Overman_rearrangement wikiPageWikiLinkText "Overman rearrangement".
- Overman_rearrangement wikiPageUsesTemplate Template:Reflist.
- Overman_rearrangement subject Category:Carboximidates.
- Overman_rearrangement subject Category:Name_reactions.
- Overman_rearrangement subject Category:Rearrangement_reactions.
- Overman_rearrangement hypernym Reaction.
- Overman_rearrangement type Disease.
- Overman_rearrangement type Group.
- Overman_rearrangement type Eponym.
- Overman_rearrangement type Group.
- Overman_rearrangement type Reaction.
- Overman_rearrangement comment "The Overman rearrangement is a chemical reaction that can be described as a Claisen rearrangement of allylic alcohols to give allylic trichloroacetamides through an imidate intermediate. The Overman rearrangement was discovered in 1974 by Larry Overman.The [3,3]-sigmatropic rearrangement is diastereoselective requires heating but can also be catalyzed by Hg(II), or Pd(II) salts.".
- Overman_rearrangement label "Overman rearrangement".
- Overman_rearrangement sameAs Q723816.
- Overman_rearrangement sameAs Overman-Umlagerung.
- Overman_rearrangement sameAs بازآرایی_اورمن.
- Overman_rearrangement sameAs Rxc3xa9arrangement_dOverman.
- Overman_rearrangement sameAs m.07vs5h.
- Overman_rearrangement sameAs ஓவர்மான்_மறுசீராக்கல்_வினை.
- Overman_rearrangement sameAs Q723816.
- Overman_rearrangement sameAs Overman重排反应.
- Overman_rearrangement wasDerivedFrom Overman_rearrangement?oldid=617785519.
- Overman_rearrangement depiction Overman_Rearrangement_scheme.svg.
- Overman_rearrangement isPrimaryTopicOf Overman_rearrangement.