237765-35-4Relevant articles and documents
A second-generation cycloaddition route to 5-substituted 3-acyltetramic acids
Jones, Raymond C. F.,Dawson, Claire E.,O'Mahony, Mary J.
, p. 873 - 876 (2007/10/03)
The 1,3-dipolar cycloaddition of α-aminonitrile oxides, formed from α- amino-acids, to enamines of β-ketoesters affords 3-(1-aminoalkyl)isoxazole- 4-carboxylic esters that are convened via pyrrolo[3,4-c]isoxazol-4-ones into 5-substituted 3-acetyltetramic