Products from heterodiene synthesis and 1,3-cycloaddition in the reaction of N,N-disubstituted 2-aminooxazoles with maleimide

DOI: 10.1007/BF02290850

Source and publish data:

Chemistry of Heterocyclic Compounds p. 584 - 592 (2000)

Update date:2022-08-04

Topics:

Authors:

Kondrat'eva

Aitzhanova

Bogdanov

Stashina

Sedishev

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Article abstract of DOI:10.1007/BF02290850

N,N-Disubstituted 2-aminooxazoles react with maleimide in two directions: heterodiene synthesis with the formation of imides of 2-aminopyridine-3,4-dicarboxylic acids and/or 1,3-cycloaddition, forming imides of 2-amino-5-acyl-Δ¹-pyrrolidine-3,4-dicarboxylic acids.

Full text of DOI:10.1007/BF02290850

Products guided by the article

Product name:4,5-dimethyl-2-(N-methyl-N-phenylamino)oxazole

Cas No:73777-31-8

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