N-Allyl-1,3-oxazines via a facile keto-ene/cyclization tandem reaction

Abstract

The intramolecular keto-ene/cyclization tandem reaction of γ- N-allylamino ketones is an effective means of producing 1,3-oxazines. The reaction usually requires high temperatures and/or pressures. We discovered that N, N-diallyl amines undergo the reaction at lower temperatures than their monoallyl analogs. An extreme example, 1- N, N-diallylamino-9,10-anthraquinone, undergoes the keto-ene reaction near ambient temperature. In the case of 1- N, N′-dialkylaminoanthraquinones, electron deficient ene components can even be used, allowing the preparation of a broad spectrum of oxazines. Furthermore, the N-allyl-1,3-oxazine can be easily deallylated to produce a 1,3-oxazine that contains a secondary amine.