Matches in DBpedia 2016-04 for { <http://dbpedia.org/resource/Lossen_rearrangement> ?p ?o }
Showing triples 1 to 48 of
48
with 100 triples per page.
- Lossen_rearrangement abstract "The Lossen rearrangement is the conversion of a betaxamic acid (1) to an isocyanate (3) via the formation of an O-acyl, sulfonyl, or phosphoryl intermediate hydroxamic acid O-derivative (2) and then conversion to its conjugate base. Here, 4-toluenesulfonyl chloride is used to form a sulfonyl Ortho-derivative of hydroxamic acid.The isocyanate can be used further to generate ureas in the presence of amines (4) or generate amines in the presence of H2O (5).".
- Lossen_rearrangement thumbnail Lossen_Rearrangement_Scheme.png?width=300.
- Lossen_rearrangement wikiPageExternalLink watch?v=0-hbqMzgxw0.
- Lossen_rearrangement wikiPageID "4042556".
- Lossen_rearrangement wikiPageLength "3349".
- Lossen_rearrangement wikiPageOutDegree "16".
- Lossen_rearrangement wikiPageRevisionID "702026382".
- Lossen_rearrangement wikiPageWikiLink 4-Toluenesulfonyl_chloride.
- Lossen_rearrangement wikiPageWikiLink Amine.
- Lossen_rearrangement wikiPageWikiLink Betaxamic_acid.
- Lossen_rearrangement wikiPageWikiLink Carbon_dioxide.
- Lossen_rearrangement wikiPageWikiLink Category:Name_reactions.
- Lossen_rearrangement wikiPageWikiLink Category:Rearrangement_reactions.
- Lossen_rearrangement wikiPageWikiLink Curtius_rearrangement.
- Lossen_rearrangement wikiPageWikiLink Decarboxylation.
- Lossen_rearrangement wikiPageWikiLink Ester.
- Lossen_rearrangement wikiPageWikiLink Gabapentin.
- Lossen_rearrangement wikiPageWikiLink Hofmann_rearrangement.
- Lossen_rearrangement wikiPageWikiLink Isocyanate.
- Lossen_rearrangement wikiPageWikiLink Schmidt_reaction.
- Lossen_rearrangement wikiPageWikiLink File:IsocyanateGOES.png.
- Lossen_rearrangement wikiPageWikiLink File:LossenRearangmentCHEMDRAW.jpg.
- Lossen_rearrangement wikiPageWikiLink File:Lossen_Rearrangement_Scheme.png.
- Lossen_rearrangement wikiPageWikiLinkText "Lossen rearrangement".
- Lossen_rearrangement wikiPageWikiLinkText "Lossen".
- Lossen_rearrangement wikiPageUsesTemplate Template:Cite_web.
- Lossen_rearrangement wikiPageUsesTemplate Template:Reflist.
- Lossen_rearrangement wikiPageUsesTemplate Template:Use_dmy_dates.
- Lossen_rearrangement subject Category:Name_reactions.
- Lossen_rearrangement subject Category:Rearrangement_reactions.
- Lossen_rearrangement hypernym Conversion.
- Lossen_rearrangement type VideoGame.
- Lossen_rearrangement type Eponym.
- Lossen_rearrangement type Reaction.
- Lossen_rearrangement comment "The Lossen rearrangement is the conversion of a betaxamic acid (1) to an isocyanate (3) via the formation of an O-acyl, sulfonyl, or phosphoryl intermediate hydroxamic acid O-derivative (2) and then conversion to its conjugate base. Here, 4-toluenesulfonyl chloride is used to form a sulfonyl Ortho-derivative of hydroxamic acid.The isocyanate can be used further to generate ureas in the presence of amines (4) or generate amines in the presence of H2O (5).".
- Lossen_rearrangement label "Lossen rearrangement".
- Lossen_rearrangement sameAs Q723650.
- Lossen_rearrangement sameAs Lossen-Abbau.
- Lossen_rearrangement sameAs Réarrangement_de_Lossen.
- Lossen_rearrangement sameAs ロッセン転位.
- Lossen_rearrangement sameAs m.0bf2zb.
- Lossen_rearrangement sameAs Перегруппировка_Лоссена.
- Lossen_rearrangement sameAs Перегрупування_Лоссена.
- Lossen_rearrangement sameAs Q723650.
- Lossen_rearrangement sameAs 洛森重排反应.
- Lossen_rearrangement wasDerivedFrom Lossen_rearrangement?oldid=702026382.
- Lossen_rearrangement depiction Lossen_Rearrangement_Scheme.png.
- Lossen_rearrangement isPrimaryTopicOf Lossen_rearrangement.