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- Blaise_reaction abstract "The Blaise reaction is an organic reaction that forms a β-ketoester from the reaction of zinc metal with a α-bromoester and a nitrile. The reaction was first reported by Edmond Blaise (1872-1939) in 1901. The final intermediate is a metaloimine, which is then hydrolyzed to give the desired β-ketoester.Bulky aliphatic esters tend to give higher yields. Steven Hannick and Yoshito Kishi have developed an improved procedure.It has been noted that free hydroxyl groups can be tolerated in the course of this reaction, which is surprising for reactions of organometallic halides.".
- Blaise_reaction thumbnail Blaise_Reaction_Scheme.png?width=300.
- Blaise_reaction wikiPageExternalLink blaise-reaction.shtm.
- Blaise_reaction wikiPageExternalLink prep.asp?prep=cv4p0120.
- Blaise_reaction wikiPageID "2031464".
- Blaise_reaction wikiPageLength "2773".
- Blaise_reaction wikiPageOutDegree "21".
- Blaise_reaction wikiPageRevisionID "685373355".
- Blaise_reaction wikiPageWikiLink Aliphatic_compound.
- Blaise_reaction wikiPageWikiLink Blaise_ketone_synthesis.
- Blaise_reaction wikiPageWikiLink Category:Addition_reactions.
- Blaise_reaction wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
- Blaise_reaction wikiPageWikiLink Category:Name_reactions.
- Blaise_reaction wikiPageWikiLink Haloketone.
- Blaise_reaction wikiPageWikiLink Hydrolysis.
- Blaise_reaction wikiPageWikiLink Journal_of_Organic_Chemistry.
- Blaise_reaction wikiPageWikiLink Journal_of_the_American_Chemical_Society.
- Blaise_reaction wikiPageWikiLink Nitrile.
- Blaise_reaction wikiPageWikiLink Organic_Syntheses.
- Blaise_reaction wikiPageWikiLink Organic_reaction.
- Blaise_reaction wikiPageWikiLink Reformatsky_reaction.
- Blaise_reaction wikiPageWikiLink Synlett.
- Blaise_reaction wikiPageWikiLink Tetrahedron_(journal).
- Blaise_reaction wikiPageWikiLink Yoshito_Kishi.
- Blaise_reaction wikiPageWikiLink Zinc.
- Blaise_reaction wikiPageWikiLink File:BlaiseRxnMech.svg.
- Blaise_reaction wikiPageWikiLink File:Blaise_Reaction_Scheme.png.
- Blaise_reaction wikiPageWikiLinkText "Blaise reaction".
- Blaise_reaction wikiPageUsesTemplate Template:DOI.
- Blaise_reaction wikiPageUsesTemplate Template:Note.
- Blaise_reaction wikiPageUsesTemplate Template:Ref.
- Blaise_reaction subject Category:Addition_reactions.
- Blaise_reaction subject Category:Carbon-carbon_bond_forming_reactions.
- Blaise_reaction subject Category:Name_reactions.
- Blaise_reaction hypernym Reaction.
- Blaise_reaction type Disease.
- Blaise_reaction type Eponym.
- Blaise_reaction type Reaction.
- Blaise_reaction comment "The Blaise reaction is an organic reaction that forms a β-ketoester from the reaction of zinc metal with a α-bromoester and a nitrile. The reaction was first reported by Edmond Blaise (1872-1939) in 1901. The final intermediate is a metaloimine, which is then hydrolyzed to give the desired β-ketoester.Bulky aliphatic esters tend to give higher yields.".
- Blaise_reaction label "Blaise reaction".
- Blaise_reaction sameAs Q1992165.
- Blaise_reaction sameAs تفاعل_بليز.
- Blaise_reaction sameAs Reacción_de_Blaise.
- Blaise_reaction sameAs واکنش_بلیز.
- Blaise_reaction sameAs Blaise-reactie.
- Blaise_reaction sameAs m.06gfj4.
- Blaise_reaction sameAs Q1992165.
- Blaise_reaction sameAs 布莱斯反应.
- Blaise_reaction wasDerivedFrom Blaise_reaction?oldid=685373355.
- Blaise_reaction depiction Blaise_Reaction_Scheme.png.
- Blaise_reaction isPrimaryTopicOf Blaise_reaction.