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- Letts_nitrile_synthesis abstract "The Letts nitrile synthesis is a chemical reaction of aromatic carboxylic acids with metal thiocyanates to form nitriles. The reaction includes the loss of carbon dioxide and potassium hydrosulfide. The polar basic substitution reaction was discovered in 1872 by Edmund A. Letts.".
- Letts_nitrile_synthesis thumbnail Letts_nitrile_synthesis_V.1.png?width=300.
- Letts_nitrile_synthesis wikiPageID "5900402".
- Letts_nitrile_synthesis wikiPageLength "7939".
- Letts_nitrile_synthesis wikiPageOutDegree "58".
- Letts_nitrile_synthesis wikiPageRevisionID "703425146".
- Letts_nitrile_synthesis wikiPageWikiLink Acetamide.
- Letts_nitrile_synthesis wikiPageWikiLink Acetic_acid.
- Letts_nitrile_synthesis wikiPageWikiLink Amide.
- Letts_nitrile_synthesis wikiPageWikiLink Antidepressant.
- Letts_nitrile_synthesis wikiPageWikiLink Aromatase_inhibitor.
- Letts_nitrile_synthesis wikiPageWikiLink Aromaticity.
- Letts_nitrile_synthesis wikiPageWikiLink Base_(chemistry).
- Letts_nitrile_synthesis wikiPageWikiLink Benzonitrile.
- Letts_nitrile_synthesis wikiPageWikiLink Benzoyl_chloride.
- Letts_nitrile_synthesis wikiPageWikiLink Breast_cancer.
- Letts_nitrile_synthesis wikiPageWikiLink Carbon_dioxide.
- Letts_nitrile_synthesis wikiPageWikiLink Carbonyl_sulfide.
- Letts_nitrile_synthesis wikiPageWikiLink Carboxylic_acid.
- Letts_nitrile_synthesis wikiPageWikiLink Catalysis.
- Letts_nitrile_synthesis wikiPageWikiLink Category:Name_reactions.
- Letts_nitrile_synthesis wikiPageWikiLink Category:Substitution_reactions.
- Letts_nitrile_synthesis wikiPageWikiLink Chemical_polarity.
- Letts_nitrile_synthesis wikiPageWikiLink Chemical_reaction.
- Letts_nitrile_synthesis wikiPageWikiLink Conjugate_acid.
- Letts_nitrile_synthesis wikiPageWikiLink Cyanation.
- Letts_nitrile_synthesis wikiPageWikiLink Cyanide.
- Letts_nitrile_synthesis wikiPageWikiLink Double_bond.
- Letts_nitrile_synthesis wikiPageWikiLink Dry_distillation.
- Letts_nitrile_synthesis wikiPageWikiLink Enantioselective_synthesis.
- Letts_nitrile_synthesis wikiPageWikiLink Fadrozole.
- Letts_nitrile_synthesis wikiPageWikiLink Fluvoxamine.
- Letts_nitrile_synthesis wikiPageWikiLink Hugo_Schiff.
- Letts_nitrile_synthesis wikiPageWikiLink Kolbe_nitrile_synthesis.
- Letts_nitrile_synthesis wikiPageWikiLink Lead(II)_thiocyanate.
- Letts_nitrile_synthesis wikiPageWikiLink Lewis_acids_and_bases.
- Letts_nitrile_synthesis wikiPageWikiLink Ligand.
- Letts_nitrile_synthesis wikiPageWikiLink Metal.
- Letts_nitrile_synthesis wikiPageWikiLink Nickel.
- Letts_nitrile_synthesis wikiPageWikiLink Nitrile.
- Letts_nitrile_synthesis wikiPageWikiLink Pinner_reaction.
- Letts_nitrile_synthesis wikiPageWikiLink Polymer.
- Letts_nitrile_synthesis wikiPageWikiLink Potassium.
- Letts_nitrile_synthesis wikiPageWikiLink Potassium_cyanide.
- Letts_nitrile_synthesis wikiPageWikiLink Potassium_hydrosulfide.
- Letts_nitrile_synthesis wikiPageWikiLink Reaction_mechanism.
- Letts_nitrile_synthesis wikiPageWikiLink Reagent.
- Letts_nitrile_synthesis wikiPageWikiLink Resonance_(chemistry).
- Letts_nitrile_synthesis wikiPageWikiLink Ritter_reaction.
- Letts_nitrile_synthesis wikiPageWikiLink Rosenmund–von_Braun_reaction.
- Letts_nitrile_synthesis wikiPageWikiLink Sigma_bond.
- Letts_nitrile_synthesis wikiPageWikiLink Solvent.
- Letts_nitrile_synthesis wikiPageWikiLink Stephen_aldehyde_synthesis.
- Letts_nitrile_synthesis wikiPageWikiLink Substitution_reaction.
- Letts_nitrile_synthesis wikiPageWikiLink Thiocyanate.
- Letts_nitrile_synthesis wikiPageWikiLink Thiocyanic_acid.
- Letts_nitrile_synthesis wikiPageWikiLink Transition_metal.
- Letts_nitrile_synthesis wikiPageWikiLink Zinc.
- Letts_nitrile_synthesis wikiPageWikiLink File:CHEM_342.png.
- Letts_nitrile_synthesis wikiPageWikiLink File:Letts_nitrile_synthesis_V.1.png.
- Letts_nitrile_synthesis wikiPageWikiLink File:Reid_modified_Letts.png.
- Letts_nitrile_synthesis wikiPageWikiLink File:Restrosynthesis_of_Fluvoxamine.png.
- Letts_nitrile_synthesis wikiPageWikiLink File:Ritter_Reaction_Scheme.png.
- Letts_nitrile_synthesis wikiPageWikiLinkText "Letts nitrile synthesis".
- Letts_nitrile_synthesis wikiPageUsesTemplate Template:Reflist.
- Letts_nitrile_synthesis subject Category:Name_reactions.
- Letts_nitrile_synthesis subject Category:Substitution_reactions.
- Letts_nitrile_synthesis hypernym Reaction.
- Letts_nitrile_synthesis type Disease.
- Letts_nitrile_synthesis type Eponym.
- Letts_nitrile_synthesis type Reaction.
- Letts_nitrile_synthesis comment "The Letts nitrile synthesis is a chemical reaction of aromatic carboxylic acids with metal thiocyanates to form nitriles. The reaction includes the loss of carbon dioxide and potassium hydrosulfide. The polar basic substitution reaction was discovered in 1872 by Edmund A. Letts.".
- Letts_nitrile_synthesis label "Letts nitrile synthesis".
- Letts_nitrile_synthesis sameAs Q520024.
- Letts_nitrile_synthesis sameAs اصطناع_ليتس_للنتريل.
- Letts_nitrile_synthesis sameAs Letts-Nitrilsynthese.
- Letts_nitrile_synthesis sameAs Síntesis_de_nitrilos_de_Letts.
- Letts_nitrile_synthesis sameAs Letts-nitrilsynthese.
- Letts_nitrile_synthesis sameAs m.0fcmc0.
- Letts_nitrile_synthesis sameAs Q520024.
- Letts_nitrile_synthesis sameAs Letts腈合成.
- Letts_nitrile_synthesis wasDerivedFrom Letts_nitrile_synthesis?oldid=703425146.
- Letts_nitrile_synthesis depiction Letts_nitrile_synthesis_V.1.png.
- Letts_nitrile_synthesis isPrimaryTopicOf Letts_nitrile_synthesis.