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- Liebeskind–Srogl_coupling abstract "The Liebeskind–Srogl coupling reaction is an organic reaction forming a new carbon–carbon bond from a thioester and a boronic acid using a metal catalyst. This reaction was invented and named after Jiri Srogl from the Academy of Sciences, Czech Republic, and Lanny S. Liebeskind from Emory University, Atlanta, Georgia, USA. The metal catalyst depicted below uses TFP = tris(2-furyl)phosphine as an additional ligand and CuTC = copper(I) thiophene-2-carboxylate as a co-metal catalyst. The overall reaction scheme is shown below.".
- Liebeskind–Srogl_coupling thumbnail Liebeskind-Strogl_coupling2.png?width=300.
- Liebeskind–Srogl_coupling wikiPageID "21599120".
- Liebeskind–Srogl_coupling wikiPageLength "2549".
- Liebeskind–Srogl_coupling wikiPageOutDegree "17".
- Liebeskind–Srogl_coupling wikiPageRevisionID "573230973".
- Liebeskind–Srogl_coupling wikiPageWikiLink Boronic_acid.
- Liebeskind–Srogl_coupling wikiPageWikiLink Carbon–carbon_bond.
- Liebeskind–Srogl_coupling wikiPageWikiLink Carbon–sulfur_bond.
- Liebeskind–Srogl_coupling wikiPageWikiLink Catalysis.
- Liebeskind–Srogl_coupling wikiPageWikiLink Catalyst.
- Liebeskind–Srogl_coupling wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
- Liebeskind–Srogl_coupling wikiPageWikiLink Category:Name_reactions.
- Liebeskind–Srogl_coupling wikiPageWikiLink Copper(I)-thiophene-2-carboxylate.
- Liebeskind–Srogl_coupling wikiPageWikiLink Emory_University.
- Liebeskind–Srogl_coupling wikiPageWikiLink Organic_reaction.
- Liebeskind–Srogl_coupling wikiPageWikiLink Organopalladium.
- Liebeskind–Srogl_coupling wikiPageWikiLink Organosulfur_compounds.
- Liebeskind–Srogl_coupling wikiPageWikiLink Oxidative_addition.
- Liebeskind–Srogl_coupling wikiPageWikiLink Oxidative_insertion.
- Liebeskind–Srogl_coupling wikiPageWikiLink Reaction_mechanism.
- Liebeskind–Srogl_coupling wikiPageWikiLink Reductive_elimination.
- Liebeskind–Srogl_coupling wikiPageWikiLink Thioester.
- Liebeskind–Srogl_coupling wikiPageWikiLink Transmetalation.
- Liebeskind–Srogl_coupling wikiPageWikiLink Transmetallation.
- Liebeskind–Srogl_coupling wikiPageWikiLink File:Liebeskind-Strogl_coupling2.png.
- Liebeskind–Srogl_coupling wikiPageWikiLink File:Liebeskind-Strogl_mechanism.png.
- Liebeskind–Srogl_coupling wikiPageWikiLinkText "Liebeskind–Srogl coupling".
- Liebeskind–Srogl_coupling hasPhotoCollection Liebeskind–Srogl_coupling.
- Liebeskind–Srogl_coupling wikiPageUsesTemplate Template:Reflist.
- Liebeskind–Srogl_coupling wikiPageUsesTemplate Template:Use_dmy_dates.
- Liebeskind–Srogl_coupling subject Category:Carbon-carbon_bond_forming_reactions.
- Liebeskind–Srogl_coupling subject Category:Name_reactions.
- Liebeskind–Srogl_coupling comment "The Liebeskind–Srogl coupling reaction is an organic reaction forming a new carbon–carbon bond from a thioester and a boronic acid using a metal catalyst. This reaction was invented and named after Jiri Srogl from the Academy of Sciences, Czech Republic, and Lanny S. Liebeskind from Emory University, Atlanta, Georgia, USA. The metal catalyst depicted below uses TFP = tris(2-furyl)phosphine as an additional ligand and CuTC = copper(I) thiophene-2-carboxylate as a co-metal catalyst.".
- Liebeskind–Srogl_coupling label "Liebeskind–Srogl coupling".
- Liebeskind–Srogl_coupling sameAs جفتشدن_لیبسکایند–اسروگل.
- Liebeskind–Srogl_coupling sameAs m.05mwkzm.
- Liebeskind–Srogl_coupling sameAs Q6543886.
- Liebeskind–Srogl_coupling sameAs Q6543886.
- Liebeskind–Srogl_coupling sameAs Liebeskind–Srogl偶联反应.
- Liebeskind–Srogl_coupling wasDerivedFrom Liebeskind–Srogl_coupling?oldid=573230973.
- Liebeskind–Srogl_coupling depiction Liebeskind-Strogl_coupling2.png.
- Liebeskind–Srogl_coupling isPrimaryTopicOf Liebeskind–Srogl_coupling.