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- Fukuyama_coupling abstract "The Fukuyama coupling is a coupling reaction taking place between a thioester and an organozinc halide in the presence of a palladium catalyst. The reaction product is a ketone. This reaction was discovered by Tohru Fukuyama et al. in 1998. Advantages are high chemoselectivity, mild reaction conditions and the use of less-toxic reagents.Fukuyama couplingOne advantage of this method is that the reaction stops at the ketone and does not proceed to a tertiary alcohol. In addition, the protocol is compatible with functional groups such as ketones, acetates, sulfides, aromatic bromides, chlorides and aldehydes.Original Fukuyama 1998 reactionThe reaction (interrupted) has been used in the synthesis of biotin Biotin total synthesisThis reaction was preceded by the conceptually related Fukuyama reduction.".
- Fukuyama_coupling thumbnail FukuyamaCoupling.svg?width=300.
- Fukuyama_coupling wikiPageID "15848569".
- Fukuyama_coupling wikiPageLength "2118".
- Fukuyama_coupling wikiPageOutDegree "14".
- Fukuyama_coupling wikiPageRevisionID "545158562".
- Fukuyama_coupling wikiPageWikiLink Biotin.
- Fukuyama_coupling wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
- Fukuyama_coupling wikiPageWikiLink Category:Name_reactions.
- Fukuyama_coupling wikiPageWikiLink Coupling_reaction.
- Fukuyama_coupling wikiPageWikiLink Fukuyama_reduction.
- Fukuyama_coupling wikiPageWikiLink Functional_group.
- Fukuyama_coupling wikiPageWikiLink Functional_groups.
- Fukuyama_coupling wikiPageWikiLink Ketone.
- Fukuyama_coupling wikiPageWikiLink Organozinc_compound.
- Fukuyama_coupling wikiPageWikiLink Organozinc_halide.
- Fukuyama_coupling wikiPageWikiLink Palladium.
- Fukuyama_coupling wikiPageWikiLink Thioester.
- Fukuyama_coupling wikiPageWikiLink Tohru_Fukuyama.
- Fukuyama_coupling wikiPageWikiLink File:Biotin2000_synthesis.svg.
- Fukuyama_coupling wikiPageWikiLink File:Fukuyama1998.svg.
- Fukuyama_coupling wikiPageWikiLink File:FukuyamaCoupling.svg.
- Fukuyama_coupling wikiPageWikiLinkText "Fukuyama coupling".
- Fukuyama_coupling hasPhotoCollection Fukuyama_coupling.
- Fukuyama_coupling wikiPageUsesTemplate Template:Reflist.
- Fukuyama_coupling subject Category:Carbon-carbon_bond_forming_reactions.
- Fukuyama_coupling subject Category:Name_reactions.
- Fukuyama_coupling hypernym Reaction.
- Fukuyama_coupling type Disease.
- Fukuyama_coupling type Eponym.
- Fukuyama_coupling type Reaction.
- Fukuyama_coupling comment "The Fukuyama coupling is a coupling reaction taking place between a thioester and an organozinc halide in the presence of a palladium catalyst. The reaction product is a ketone. This reaction was discovered by Tohru Fukuyama et al. in 1998. Advantages are high chemoselectivity, mild reaction conditions and the use of less-toxic reagents.Fukuyama couplingOne advantage of this method is that the reaction stops at the ketone and does not proceed to a tertiary alcohol.".
- Fukuyama_coupling label "Fukuyama coupling".
- Fukuyama_coupling sameAs جفتشدن_فوکویاما.
- Fukuyama_coupling sameAs 福山カップリング.
- Fukuyama_coupling sameAs m.03qcwzc.
- Fukuyama_coupling sameAs Q5507762.
- Fukuyama_coupling sameAs Q5507762.
- Fukuyama_coupling sameAs 福山偶联反应.
- Fukuyama_coupling wasDerivedFrom Fukuyama_coupling?oldid=545158562.
- Fukuyama_coupling depiction FukuyamaCoupling.svg.
- Fukuyama_coupling isPrimaryTopicOf Fukuyama_coupling.