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The key intermediates, \u03b2\u2010amino ketones, were obtained through tandem Meyer\u2010Schuster rearrangement reaction of propargyl alcohols and intermolecular Michael addition of \u03b1, \u03b2\u2010unsaturated ketones and sulfonamide. Then the in\u2005situ generated \u03b1\u2010halo\u2010\u03b2\u2010amino ketones underwent the base\u2010promoted intramolecular cyclization to give diverse acyl aziridines in a one\u2010pot fashion. These transformations are reliable on a large scale. 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