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- Baylis–Hillman_reaction abstract "The Baylis–Hillman reaction is a carbon-carbon bond forming reaction between the α-position of an activated alkene and an aldehyde, or generally a carbon electrophile. Employing a nucleophilic catalyst, such as tertiary amine and phosphine, this reaction provides a densely functionalized product (e.g. functionalized allyl alcohol in the case of aldehyde as the electrophile). This reaction is also known as the Morita–Baylis–Hillman reaction or MBH reaction. It is named for the Japanese chemist Ken-ichi Morita, the British chemist Anthony B. Baylis and the German chemist Melville E. D. Hillman.DABCO is one of the most frequently used tertiary amine catalysts for this reaction. In addition, nucleophilic amines such as DMAP and DBU as well as phosphines have been found to successfully catalyze this reaction.MBH reaction has several advantages as a useful synthetic method: 1) It is an atom-economic coupling of easily prepared starting materials. 2) Reaction of a pro-chiral electrophile generates a chiral center, therefore an asymmetric synthesis is possible. 3) Reaction products usually contain multiple functionalities in a proximity so that a variety of further transformations are possible. 4) It can employ a nucleophilic organo-catalytic system without the use of heavy metal under mild conditions.Several reviews have been written.".
- Baylis–Hillman_reaction thumbnail MBH_general_scheme.png?width=300.
- Baylis–Hillman_reaction wikiPageID "30862625".
- Baylis–Hillman_reaction wikiPageLength "21937".
- Baylis–Hillman_reaction wikiPageOutDegree "41".
- Baylis–Hillman_reaction wikiPageRevisionID "647305196".
- Baylis–Hillman_reaction wikiPageWikiLink 1,8-Diazabicycloundec-7-ene.
- Baylis–Hillman_reaction wikiPageWikiLink 4-Dimethylaminopyridine.
- Baylis–Hillman_reaction wikiPageWikiLink Amine.
- Baylis–Hillman_reaction wikiPageWikiLink Aza-Baylis–Hillman_reaction.
- Baylis–Hillman_reaction wikiPageWikiLink Brook_rearrangement.
- Baylis–Hillman_reaction wikiPageWikiLink Category:Addition_reactions.
- Baylis–Hillman_reaction wikiPageWikiLink Category:Carbon-carbon_bond_forming_reactions.
- Baylis–Hillman_reaction wikiPageWikiLink Category:Name_reactions.
- Baylis–Hillman_reaction wikiPageWikiLink DABCO.
- Baylis–Hillman_reaction wikiPageWikiLink DBU_(chemistry).
- Baylis–Hillman_reaction wikiPageWikiLink File:Diversonol_synthesis_by_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:ICD_MBH_asymmetric.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Intramolecular_RC_reaction.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Jacobsen_thiourea_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:La_Lewis_acid_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:MBH_Scope_Diagram.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:MBH_general_scheme.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:MBH_in_Salinosporamide_A_synthesis.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:MBH_initial_mechanism.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:MBH_revised_mechanism.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Pd_Lewis_acid_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Phosphine_squaramide_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Phosphine_thiourea_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Proline_MBH_asymmetric.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Secondary_amine_cat_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Sila_MBH_reaction.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Sultam_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Sultam_allene_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink Heterocyclic_compound.
- Baylis–Hillman_reaction wikiPageWikiLink Michael_addition.
- Baylis–Hillman_reaction wikiPageWikiLink Michael_reaction.
- Baylis–Hillman_reaction wikiPageWikiLink Multi-component_reaction.
- Baylis–Hillman_reaction wikiPageWikiLink Multicomponent_reaction.
- Baylis–Hillman_reaction wikiPageWikiLink Nucleophile.
- Baylis–Hillman_reaction wikiPageWikiLink Nucleophilic.
- Baylis–Hillman_reaction wikiPageWikiLink Phosphine.
- Baylis–Hillman_reaction wikiPageWikiLink Phosphines.
- Baylis–Hillman_reaction wikiPageWikiLink Rauhut-Currier_reaction.
- Baylis–Hillman_reaction wikiPageWikiLink Rauhut–Currier_reaction.
- Baylis–Hillman_reaction wikiPageWikiLink Squaramide.
- Baylis–Hillman_reaction wikiPageWikiLink File:3-component_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Anatoxin_MBH_synthesis.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Boron_cat_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Chiral_phosphine_aza_MBH_2.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Double_MBH_rxn.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Fu_DMAP_MBH.png.
- Baylis–Hillman_reaction wikiPageWikiLink File:Tandem_MBH_cyclization.png.
- Baylis–Hillman_reaction wikiPageWikiLinkText "Baylis–Hillman reaction".
- Baylis–Hillman_reaction hasPhotoCollection Baylis–Hillman_reaction.
- Baylis–Hillman_reaction wikiPageUsesTemplate Template:Reflist.
- Baylis–Hillman_reaction subject Category:Addition_reactions.
- Baylis–Hillman_reaction subject Category:Carbon-carbon_bond_forming_reactions.
- Baylis–Hillman_reaction subject Category:Name_reactions.
- Baylis–Hillman_reaction comment "The Baylis–Hillman reaction is a carbon-carbon bond forming reaction between the α-position of an activated alkene and an aldehyde, or generally a carbon electrophile. Employing a nucleophilic catalyst, such as tertiary amine and phosphine, this reaction provides a densely functionalized product (e.g. functionalized allyl alcohol in the case of aldehyde as the electrophile). This reaction is also known as the Morita–Baylis–Hillman reaction or MBH reaction.".
- Baylis–Hillman_reaction label "Baylis–Hillman reaction".
- Baylis–Hillman_reaction sameAs Reacció_de_Baylis-Hillman.
- Baylis–Hillman_reaction sameAs Baylis-Hillman-Reaktion.
- Baylis–Hillman_reaction sameAs Reacción_de_Baylis-Hillman.
- Baylis–Hillman_reaction sameAs Reaksi_Baylis-Hillman.
- Baylis–Hillman_reaction sameAs 森田・ベイリス・ヒルマン反応.
- Baylis–Hillman_reaction sameAs Baylis-Hillman-reactie.
- Baylis–Hillman_reaction sameAs Reakcja_Baylisa-Hillmana.
- Baylis–Hillman_reaction sameAs m.075qdd.
- Baylis–Hillman_reaction sameAs Q812563.
- Baylis–Hillman_reaction sameAs Q812563.
- Baylis–Hillman_reaction sameAs 贝里斯-希尔曼反应.
- Baylis–Hillman_reaction wasDerivedFrom Baylis–Hillman_reaction?oldid=647305196.
- Baylis–Hillman_reaction depiction MBH_general_scheme.png.
- Baylis–Hillman_reaction isPrimaryTopicOf Baylis–Hillman_reaction.