Matches in DBpedia 2015-10 for { <http://dbpedia.org/resource/Japp–Maitland_condensation> ?p ?o }
Showing triples 1 to 42 of
42
with 100 triples per page.
- Japp–Maitland_condensation abstract "The Japp–Maitland condensation is an organic reaction and a type of Aldol reaction and a tandem reaction. In a reaction between the ketone 2-pentanone and the aldehyde benzaldehyde catalyzed by base the bis Aldol adduct is formed first. The second step is a ring-closing reaction when one hydroxyl group displaces the other in a nucleophilic substitution forming an oxo-tetrahydropyran. Japp-Maitland condensationThe reaction was first described by Francis Robert Japp and William Maitland in 1904.The Japp–Maitland reaction is of some importance to synthetic organic chemistry for example as part of the synthesis of biomolecule centrolobine:Japp–Maitland condensation in centrolobine synthesis↑ ↑ ↑".
- Japp–Maitland_condensation thumbnail Maitland-Japp.svg?width=300.
- Japp–Maitland_condensation wikiPageID "22052850".
- Japp–Maitland_condensation wikiPageLength "1709".
- Japp–Maitland_condensation wikiPageOutDegree "19".
- Japp–Maitland_condensation wikiPageRevisionID "558723251".
- Japp–Maitland_condensation wikiPageWikiLink 2-Pentanone.
- Japp–Maitland_condensation wikiPageWikiLink 2-pentanone.
- Japp–Maitland_condensation wikiPageWikiLink Alcohol.
- Japp–Maitland_condensation wikiPageWikiLink Aldehyde.
- Japp–Maitland_condensation wikiPageWikiLink Aldol_reaction.
- Japp–Maitland_condensation wikiPageWikiLink Base_(chemistry).
- Japp–Maitland_condensation wikiPageWikiLink Benzaldehyde.
- Japp–Maitland_condensation wikiPageWikiLink Biomolecule.
- Japp–Maitland_condensation wikiPageWikiLink Cascade_reaction.
- Japp–Maitland_condensation wikiPageWikiLink Catalysis.
- Japp–Maitland_condensation wikiPageWikiLink Category:Name_reactions.
- Japp–Maitland_condensation wikiPageWikiLink Cyclic_compound.
- Japp–Maitland_condensation wikiPageWikiLink Francis_Robert_Japp.
- Japp–Maitland_condensation wikiPageWikiLink Ketone.
- Japp–Maitland_condensation wikiPageWikiLink Nucleophilic_substitution.
- Japp–Maitland_condensation wikiPageWikiLink Organic_reaction.
- Japp–Maitland_condensation wikiPageWikiLink Ring-closing_reaction.
- Japp–Maitland_condensation wikiPageWikiLink Tandem_reaction.
- Japp–Maitland_condensation wikiPageWikiLink Tetrahydropyran.
- Japp–Maitland_condensation wikiPageWikiLink William_Maitland_(chemist).
- Japp–Maitland_condensation wikiPageWikiLink File:Maitland-Japp.svg.
- Japp–Maitland_condensation wikiPageWikiLink File:Maitland-Japp_application.svg.
- Japp–Maitland_condensation wikiPageWikiLinkText "Japp–Maitland condensation".
- Japp–Maitland_condensation hasPhotoCollection Japp–Maitland_condensation.
- Japp–Maitland_condensation wikiPageUsesTemplate Template:Reflist.
- Japp–Maitland_condensation wikiPageUsesTemplate Template:Use_dmy_dates.
- Japp–Maitland_condensation subject Category:Name_reactions.
- Japp–Maitland_condensation comment "The Japp–Maitland condensation is an organic reaction and a type of Aldol reaction and a tandem reaction. In a reaction between the ketone 2-pentanone and the aldehyde benzaldehyde catalyzed by base the bis Aldol adduct is formed first. The second step is a ring-closing reaction when one hydroxyl group displaces the other in a nucleophilic substitution forming an oxo-tetrahydropyran.".
- Japp–Maitland_condensation label "Japp–Maitland condensation".
- Japp–Maitland_condensation sameAs m.05p2h2l.
- Japp–Maitland_condensation sameAs Q6159350.
- Japp–Maitland_condensation sameAs Q6159350.
- Japp–Maitland_condensation sameAs Japp–Maitland缩合反应.
- Japp–Maitland_condensation wasDerivedFrom Japp–Maitland_condensation?oldid=558723251.
- Japp–Maitland_condensation depiction Maitland-Japp.svg.
- Japp–Maitland_condensation isPrimaryTopicOf Japp–Maitland_condensation.