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- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis abstract "The Erlenmeyer–Plöchl azlactone and amino acid synthesis, named after Friedrich Gustav Carl Emil Erlenmeyer who partly discovered the reaction, is a series of chemical reactions which transform glycine to various other amino acids via an oxazolone and an azlactone.Hippuric acid cyclizes in the presence of acetic anhydride, condensing to give 2-phenyl-oxazolone. This intermediate also has two acidic protons and reacts with benzaldehyde, acetic anhydride and sodium acetate to a so-called azlactone. This compound on reduction gives access to phenylalanine.".
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis thumbnail AzlactoneChemistry.png?width=300.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageID "11259102".
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageLength "4336".
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageOutDegree "23".
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageRevisionID "701934074".
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Acetic_anhydride.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Amino_acid.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Benzaldehyde.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Category:Condensation_reactions.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Category:Heterocycle_forming_reactions.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Category:Name_reactions.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Chemical_reaction.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Dakin–West_reaction.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Friedrich_Gustav_Carl_Emil_Erlenmeyer.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Glycine.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Hippuric_acid.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Hydantoin.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Oxazolone.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Perkin_reaction.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Phenylalanine.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Rhodanine.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Thiohydantoin.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink Tyrosine.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink File:AzlactoneChemistry.png.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLink File:ErlenMeyerAminoAcidSynthesisTyrosine.svg.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageWikiLinkText "Erlenmeyer–Plöchl azlactone and amino-acid synthesis".
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wikiPageUsesTemplate Template:Reflist.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis subject Category:Condensation_reactions.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis subject Category:Heterocycle_forming_reactions.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis subject Category:Name_reactions.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis hypernym Series.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis type TelevisionShow.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis type Diacritic.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis type Eponym.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis type Reaction.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis type Redirect.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis comment "The Erlenmeyer–Plöchl azlactone and amino acid synthesis, named after Friedrich Gustav Carl Emil Erlenmeyer who partly discovered the reaction, is a series of chemical reactions which transform glycine to various other amino acids via an oxazolone and an azlactone.Hippuric acid cyclizes in the presence of acetic anhydride, condensing to give 2-phenyl-oxazolone.".
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis label "Erlenmeyer–Plöchl azlactone and amino-acid synthesis".
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis sameAs Q844476.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis sameAs Erlenmeyer-Synthese.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis sameAs Síntesis_de_aminoácidos_de_Erlenmeyer-Plöchl.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis sameAs エルレンマイヤー・プロッフルのアズラクトンとアミノ酸合成.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis sameAs m.03bxygn.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis sameAs Q844476.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis sameAs Erlenmeyer–Plöchl吖内酯及氨基酸合成.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis wasDerivedFrom Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis?oldid=701934074.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis depiction AzlactoneChemistry.png.
- Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis isPrimaryTopicOf Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis.