Stereoselective synthesis of 2-pyrrolinyl- and 2-imidazolinylthiazoles

Mendeleev Communications Pub Date: DOI: 10.1070/MC1999v009n03ABEH001082

Abstract

The reaction of 2-isocyanomethylthiazoles with trans-chalcone or aromatic azomethines in the presence of copper compounds results in only trans-pyrrolines or trans-imidazolines with thiazole substituents, as evidenced by 1H NMR and mass spectrometry.

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