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- Kiliani–Fischer_synthesis abstract "The Kiliani–Fischer synthesis, named for German chemists Heinrich Kiliani and Hermann Emil Fischer, is a method for synthesizing monosaccharides. It proceeds via synthesis and hydrolysis of a cyanohydrin, thus elongating the carbon chain of an aldose by one carbon atom while preserving stereochemistry on all the previously present chiral carbons. The new chiral carbon is produced with both stereochemistries, so the product of a Kiliani–Fischer synthesis is a mixture of two diastereomeric sugars, called epimers. For example, D-arabinose is converted to a mixture of D-glucose and D-mannose.".
- Kiliani–Fischer_synthesis thumbnail Kiliani-Fischer_synthesis.png?width=300.
- Kiliani–Fischer_synthesis wikiPageID "6364894".
- Kiliani–Fischer_synthesis wikiPageLength "6709".
- Kiliani–Fischer_synthesis wikiPageOutDegree "77".
- Kiliani–Fischer_synthesis wikiPageRevisionID "674376565".
- Kiliani–Fischer_synthesis wikiPageWikiLink Aldehyde.
- Kiliani–Fischer_synthesis wikiPageWikiLink Alditol.
- Kiliani–Fischer_synthesis wikiPageWikiLink Aldol_addition.
- Kiliani–Fischer_synthesis wikiPageWikiLink Aldol_reaction.
- Kiliani–Fischer_synthesis wikiPageWikiLink Aldonic_acid.
- Kiliani–Fischer_synthesis wikiPageWikiLink Aldose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Aldoses.
- Kiliani–Fischer_synthesis wikiPageWikiLink Arabinose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Barium_sulfate.
- Kiliani–Fischer_synthesis wikiPageWikiLink Carbonyl.
- Kiliani–Fischer_synthesis wikiPageWikiLink Carboxylic_acid.
- Kiliani–Fischer_synthesis wikiPageWikiLink Catalysis.
- Kiliani–Fischer_synthesis wikiPageWikiLink Catalyst.
- Kiliani–Fischer_synthesis wikiPageWikiLink Category:Addition_reactions.
- Kiliani–Fischer_synthesis wikiPageWikiLink Category:Name_reactions.
- Kiliani–Fischer_synthesis wikiPageWikiLink Category:Organic_redox_reactions.
- Kiliani–Fischer_synthesis wikiPageWikiLink Chemical_equilibrium.
- Kiliani–Fischer_synthesis wikiPageWikiLink Chemical_yield.
- Kiliani–Fischer_synthesis wikiPageWikiLink Chirality_(chemistry).
- Kiliani–Fischer_synthesis wikiPageWikiLink Chromatography.
- Kiliani–Fischer_synthesis wikiPageWikiLink Cyanide.
- Kiliani–Fischer_synthesis wikiPageWikiLink Cyanohydrin.
- Kiliani–Fischer_synthesis wikiPageWikiLink Cyclic_compound.
- Kiliani–Fischer_synthesis wikiPageWikiLink Diastereomer.
- Kiliani–Fischer_synthesis wikiPageWikiLink Enediol.
- Kiliani–Fischer_synthesis wikiPageWikiLink Enol.
- Kiliani–Fischer_synthesis wikiPageWikiLink Epimer.
- Kiliani–Fischer_synthesis wikiPageWikiLink Fructose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Germany.
- Kiliani–Fischer_synthesis wikiPageWikiLink Glucono_delta-lactone.
- Kiliani–Fischer_synthesis wikiPageWikiLink Gluconolactone.
- Kiliani–Fischer_synthesis wikiPageWikiLink Glucononitrile.
- Kiliani–Fischer_synthesis wikiPageWikiLink Glucose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Hemiacetal.
- Kiliani–Fischer_synthesis wikiPageWikiLink Heptose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Hermann_Emil_Fischer.
- Kiliani–Fischer_synthesis wikiPageWikiLink Hexose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Homologation_reaction.
- Kiliani–Fischer_synthesis wikiPageWikiLink Homologation_reactions.
- Kiliani–Fischer_synthesis wikiPageWikiLink Hydrogen.
- Kiliani–Fischer_synthesis wikiPageWikiLink Hydrogenation.
- Kiliani–Fischer_synthesis wikiPageWikiLink Hydrolysis.
- Kiliani–Fischer_synthesis wikiPageWikiLink Hydroxyl.
- Kiliani–Fischer_synthesis wikiPageWikiLink Imine.
- Kiliani–Fischer_synthesis wikiPageWikiLink Ketone.
- Kiliani–Fischer_synthesis wikiPageWikiLink Lactone.
- Kiliani–Fischer_synthesis wikiPageWikiLink Lindlar_catalyst.
- Kiliani–Fischer_synthesis wikiPageWikiLink Lindlar_palladium.
- Kiliani–Fischer_synthesis wikiPageWikiLink Lyxose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Mannonolactone.
- Kiliani–Fischer_synthesis wikiPageWikiLink Mannononitrile.
- Kiliani–Fischer_synthesis wikiPageWikiLink Mannose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Monosaccharide.
- Kiliani–Fischer_synthesis wikiPageWikiLink Monosaccharides.
- Kiliani–Fischer_synthesis wikiPageWikiLink Mutarotation.
- Kiliani–Fischer_synthesis wikiPageWikiLink Nucleophilic_addition.
- Kiliani–Fischer_synthesis wikiPageWikiLink Organic_redox_reaction.
- Kiliani–Fischer_synthesis wikiPageWikiLink Organic_reduction.
- Kiliani–Fischer_synthesis wikiPageWikiLink Organic_synthesis.
- Kiliani–Fischer_synthesis wikiPageWikiLink Palladium.
- Kiliani–Fischer_synthesis wikiPageWikiLink Pentose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Poisoned_catalysts.
- Kiliani–Fischer_synthesis wikiPageWikiLink Polyol.
- Kiliani–Fischer_synthesis wikiPageWikiLink Separation_process.
- Kiliani–Fischer_synthesis wikiPageWikiLink Sodium_amalgam.
- Kiliani–Fischer_synthesis wikiPageWikiLink Solvent.
- Kiliani–Fischer_synthesis wikiPageWikiLink Stereochemistry.
- Kiliani–Fischer_synthesis wikiPageWikiLink Tetrose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Threose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Triose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Wohl_degradation.
- Kiliani–Fischer_synthesis wikiPageWikiLink Xylose.
- Kiliani–Fischer_synthesis wikiPageWikiLink Yield_(chemistry).
- Kiliani–Fischer_synthesis wikiPageWikiLink File:Family_tree_aldoses.svg.
- Kiliani–Fischer_synthesis wikiPageWikiLink File:Kiliani-FischerSynthesisEg.png.
- Kiliani–Fischer_synthesis wikiPageWikiLink File:Kiliani-Fischer_synthesis.png.
- Kiliani–Fischer_synthesis wikiPageWikiLinkText "Kiliani–Fischer synthesis".
- Kiliani–Fischer_synthesis hasPhotoCollection Kiliani–Fischer_synthesis.
- Kiliani–Fischer_synthesis subject Category:Addition_reactions.
- Kiliani–Fischer_synthesis subject Category:Name_reactions.
- Kiliani–Fischer_synthesis subject Category:Organic_redox_reactions.
- Kiliani–Fischer_synthesis comment "The Kiliani–Fischer synthesis, named for German chemists Heinrich Kiliani and Hermann Emil Fischer, is a method for synthesizing monosaccharides. It proceeds via synthesis and hydrolysis of a cyanohydrin, thus elongating the carbon chain of an aldose by one carbon atom while preserving stereochemistry on all the previously present chiral carbons.".
- Kiliani–Fischer_synthesis label "Kiliani–Fischer synthesis".
- Kiliani–Fischer_synthesis sameAs Kiliani-Fischer-Synthese.
- Kiliani–Fischer_synthesis sameAs Síntesis_de_Kiliani-Fischer.
- Kiliani–Fischer_synthesis sameAs Synthèse_de_Kiliani-Fischer.
- Kiliani–Fischer_synthesis sameAs Sintesi_di_Kiliani-Fischer.
- Kiliani–Fischer_synthesis sameAs m.0g2lqn.
- Kiliani–Fischer_synthesis sameAs Q903228.
- Kiliani–Fischer_synthesis sameAs Q903228.
- Kiliani–Fischer_synthesis sameAs 克利安尼-费歇尔合成.
- Kiliani–Fischer_synthesis wasDerivedFrom Kiliani–Fischer_synthesis?oldid=674376565.
- Kiliani–Fischer_synthesis depiction Kiliani-Fischer_synthesis.png.
- Kiliani–Fischer_synthesis isPrimaryTopicOf Kiliani–Fischer_synthesis.