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- Fukuyama_indole_synthesis abstract "The Fukuyama indole synthesis is a versatile tin mediated chemical reaction that results in the formation of 2,3-disubstituted indoles. A practical one-pot reaction that can be useful for the creation of disubstituted indoles. Most commonly tributyltin hydride is utilized as the reducing agent, with azobisisobutyronitrile (AIBN) as a radical initiator. Triethylborane can also be used as a radical initiator. The reaction can begin with either an o-isocyanostyrene or a 2-alkenylthioanilide derivative, both forming the indole through Radical cyclization via an alpha-stannoimidoyl radical. The R group can be a range of both basic and acidic sensitive functional groups such as esters, THP ethers, and beta-lactams. In addition the reaction is not stereo specific, in that both the cis and trans isoform can be used to obtain the desired product.".
- Fukuyama_indole_synthesis thumbnail Fukuyama_Indole_Synthesis_Showing_Both_Potential_Starting_Reagents.png?width=300.
- Fukuyama_indole_synthesis wikiPageID "14985642".
- Fukuyama_indole_synthesis wikiPageLength "8027".
- Fukuyama_indole_synthesis wikiPageOutDegree "29".
- Fukuyama_indole_synthesis wikiPageRevisionID "646120549".
- Fukuyama_indole_synthesis wikiPageWikiLink Alkenylthioanilide.
- Fukuyama_indole_synthesis wikiPageWikiLink Aspidophytine.
- Fukuyama_indole_synthesis wikiPageWikiLink Azobisisobutyronitrile.
- Fukuyama_indole_synthesis wikiPageWikiLink Category:Free_radical_reactions.
- Fukuyama_indole_synthesis wikiPageWikiLink Category:Indole_forming_reactions.
- Fukuyama_indole_synthesis wikiPageWikiLink Category:Name_reactions.
- Fukuyama_indole_synthesis wikiPageWikiLink Chemical_reaction.
- Fukuyama_indole_synthesis wikiPageWikiLink Heck_reaction.
- Fukuyama_indole_synthesis wikiPageWikiLink Indole.
- Fukuyama_indole_synthesis wikiPageWikiLink Metalation.
- Fukuyama_indole_synthesis wikiPageWikiLink Natural_product.
- Fukuyama_indole_synthesis wikiPageWikiLink One-pot_synthesis.
- Fukuyama_indole_synthesis wikiPageWikiLink Protecting_group.
- Fukuyama_indole_synthesis wikiPageWikiLink Radical_cyclization.
- Fukuyama_indole_synthesis wikiPageWikiLink Reaction_mechanism.
- Fukuyama_indole_synthesis wikiPageWikiLink Sonogashira_coupling.
- Fukuyama_indole_synthesis wikiPageWikiLink Stille_reaction.
- Fukuyama_indole_synthesis wikiPageWikiLink Strychnine.
- Fukuyama_indole_synthesis wikiPageWikiLink Total_synthesis.
- Fukuyama_indole_synthesis wikiPageWikiLink Tributyltin_hydride.
- Fukuyama_indole_synthesis wikiPageWikiLink Triethylborane.
- Fukuyama_indole_synthesis wikiPageWikiLink Vinblastine.
- Fukuyama_indole_synthesis wikiPageWikiLink Vinca_alkaloid.
- Fukuyama_indole_synthesis wikiPageWikiLink File:Fukuyama_Indole_Synthesis_Example_with_Iodine_as_Substituent.png.
- Fukuyama_indole_synthesis wikiPageWikiLink File:Fukuyama_Indole_Synthesis_Mechanism_with_Alkenylthioanilide_Group.png.
- Fukuyama_indole_synthesis wikiPageWikiLink File:Fukuyama_Indole_Synthesis_Mechanism_with_an_Isocyano_Group.png.
- Fukuyama_indole_synthesis wikiPageWikiLink File:Fukuyama_Indole_Synthesis_Showing_Both_Potential_Starting_Reagents.png.
- Fukuyama_indole_synthesis wikiPageWikiLink File:Possible_Next_Step_Reaction_with_2-iodoindoles.png.
- Fukuyama_indole_synthesis wikiPageWikiLink File:Sample_Fukuyama_Indole_Reaction_Step_in_the_Synthesis_of_Vinblastine.png.
- Fukuyama_indole_synthesis wikiPageWikiLinkText "Fukuyama indole synthesis".
- Fukuyama_indole_synthesis wikiPageUsesTemplate Template:Reflist.
- Fukuyama_indole_synthesis subject Category:Free_radical_reactions.
- Fukuyama_indole_synthesis subject Category:Indole_forming_reactions.
- Fukuyama_indole_synthesis subject Category:Name_reactions.
- Fukuyama_indole_synthesis hypernym Reaction.
- Fukuyama_indole_synthesis type Disease.
- Fukuyama_indole_synthesis type Eponym.
- Fukuyama_indole_synthesis type Reaction.
- Fukuyama_indole_synthesis comment "The Fukuyama indole synthesis is a versatile tin mediated chemical reaction that results in the formation of 2,3-disubstituted indoles. A practical one-pot reaction that can be useful for the creation of disubstituted indoles. Most commonly tributyltin hydride is utilized as the reducing agent, with azobisisobutyronitrile (AIBN) as a radical initiator. Triethylborane can also be used as a radical initiator.".
- Fukuyama_indole_synthesis label "Fukuyama indole synthesis".
- Fukuyama_indole_synthesis sameAs Q3118805.
- Fukuyama_indole_synthesis sameAs Síntesis_de_indoles_de_Fukuyama.
- Fukuyama_indole_synthesis sameAs Synthxc3xa8se_de_Fukuyama_dindoles.
- Fukuyama_indole_synthesis sameAs 福山インドール合成.
- Fukuyama_indole_synthesis sameAs Fukuyama-indoolsynthese.
- Fukuyama_indole_synthesis sameAs m.03h3rz5.
- Fukuyama_indole_synthesis sameAs Q3118805.
- Fukuyama_indole_synthesis sameAs 福山吲哚合成.
- Fukuyama_indole_synthesis wasDerivedFrom Fukuyama_indole_synthesis?oldid=646120549.
- Fukuyama_indole_synthesis depiction Fukuyama_Indole_Synthesis_Showing_Both_Potential_Starting_Reagents.png.
- Fukuyama_indole_synthesis isPrimaryTopicOf Fukuyama_indole_synthesis.