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- Q844476 subject Q7458901.
- Q844476 subject Q8408894.
- Q844476 subject Q8509241.
- Q844476 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.".
- Q844476 thumbnail AzlactoneChemistry.png?width=300.
- Q844476 wikiPageWikiLink Q170545.
- Q844476 wikiPageWikiLink Q188017.
- Q844476 wikiPageWikiLink Q2741084.
- Q844476 wikiPageWikiLink Q36534.
- Q844476 wikiPageWikiLink Q372524.
- Q844476 wikiPageWikiLink Q407775.
- Q844476 wikiPageWikiLink Q412803.
- Q844476 wikiPageWikiLink Q418082.
- Q844476 wikiPageWikiLink Q5503807.
- Q844476 wikiPageWikiLink Q620730.
- Q844476 wikiPageWikiLink Q7115125.
- Q844476 wikiPageWikiLink Q7458901.
- Q844476 wikiPageWikiLink Q8066.
- Q844476 wikiPageWikiLink Q8408894.
- Q844476 wikiPageWikiLink Q8509241.
- Q844476 wikiPageWikiLink Q898605.
- Q844476 wikiPageWikiLink Q899912.
- Q844476 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.".
- Q844476 label "Erlenmeyer–Plöchl azlactone and amino-acid synthesis".
- Q844476 depiction AzlactoneChemistry.png.