Preparation and reactions of some o-dialkylaminoarylmethylene-substituted azlactones (oxazol-5-ones)

Abstract
Various azlactones derived from o-dialkylaminobenzaldehydes were treated with nucleophiles (aqueous ethanolic sodium hydroxide, amines, and Grignard reagents). The carbinols obtained by reaction with a Grignard reagent were cyclised to give the corresponding indenes (5).

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