The Martinet dioxindole synthesis was first reported in 1913 by J. Martinet.[1] It is a chemical reaction in which a primary or secondary aniline or substituted aromatic amine is condensed with ethyl or methyl ester of mesoxalic acid to make a dioxindole in the absence of oxygen.[2]
^Guyot A, Martinet J (1913). "Formation of derivatives of dioxindole from esters of mesoxalic acid and aromatic amines or amino quinolines". Compt. Rend. 156: 1625.
^Sumpter, Ward C. (1945). "The Chemistry of Oxindole". Chemical Reviews. 37 (3): 443–479. doi:10.1021/cr60118a003. ISSN 0009-2665. PMID 21013427.
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The Martinetdioxindolesynthesis was first reported in 1913 by J. Martinet. It is a chemical reaction in which a primary or secondary aniline or substituted...