A preparation of methyl 2-amino-3-formylbenzoate and its use in Friedlander synthesis

Article abstract of DOI:10.1080/00397919908085895

The title compound has been prepared in four steps from methyl isatin-7- carboxylate. Condensations with 1-indanone and analogs gave 11H-indeno[1,2- b]quinoline-6-carboxylic acids, and with cyclohexanones gave acridine-4- carboxylic acids.

Full text of DOI:10.1080/00397919908085895

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A Preparation Of Methyl 2-amino-3-
formylbenzoate and its use in
Friedlander Synthesis
Xianyong Bu a & Leslie W. Deady a
a Department of Chemistry, La Trobe University, Bundoora,
Victoria, 3083, Australia
Version of record first published: 17 Sep 2007.
To cite this article: Xianyong Bu & Leslie W. Deady (1999): A Preparation Of Methyl 2-
amino-3-formylbenzoate and its use in Friedlander Synthesis, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry, 29:23,
4223-4233
To link to this article: http://dx.doi.org/10.1080/00397919908085895
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