Microwave irradiation of chloroacetylarenes and enamines induced an aza-Darzens reaction followed by rearrangement of the aziridinium intermediate to give (2-amino-3-alkenoyl)arenes that were reduced selectively to syn-β-aminoalcohols as pseudo-ephedrine analogues.
氯代
乙酰苯与烯
胺类的微波辐射诱导了氮杂Darzens反应,接着氮杂环丙鎓中间体的重排,得到了二氧化
氨基-三碳烯酰苯类化合物,这类化合物被选择性地还原为伪
麻黄碱的伪手性β-
氨基
醇类似物。