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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 a 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 wikiPageRevisionID "591179335".
- Fukuyama_indole_synthesis hasPhotoCollection Fukuyama_indole_synthesis.
- 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 type ChemicalProcess113446390.
- Fukuyama_indole_synthesis type ChemicalReaction113447361.
- Fukuyama_indole_synthesis type FreeRadicalReactions.
- Fukuyama_indole_synthesis type NameReactions.
- Fukuyama_indole_synthesis type NaturalProcess113518963.
- Fukuyama_indole_synthesis type PhysicalEntity100001930.
- Fukuyama_indole_synthesis type Process100029677.
- 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 label "Fukuyama-indoolsynthese".
- Fukuyama_indole_synthesis label "Synthèse de Fukuyama d'indoles".
- Fukuyama_indole_synthesis label "Síntesis de indoles de Fukuyama".
- Fukuyama_indole_synthesis label "福山インドール合成".
- Fukuyama_indole_synthesis label "福山吲哚合成".
- Fukuyama_indole_synthesis sameAs Síntesis_de_indoles_de_Fukuyama.
- Fukuyama_indole_synthesis sameAs Synthèse_de_Fukuyama_d'indoles.
- 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 Q3118805.
- Fukuyama_indole_synthesis sameAs Fukuyama_indole_synthesis.
- Fukuyama_indole_synthesis wasDerivedFrom Fukuyama_indole_synthesis?oldid=591179335.
- Fukuyama_indole_synthesis depiction Fukuyama_Indole_Synthesis_Showing_Both_Potential_Starting_Reagents.png.
- Fukuyama_indole_synthesis isPrimaryTopicOf Fukuyama_indole_synthesis.