Diphenylphosphinoylallenes containing a ClCH2 group were synthesized, and their reaction with cytisine was studied. It was shown that the reaction involves exclusives as nucleophilic substitution of chlorine in the chloromethyl group. The synthesized conjugates of cytisine with diphenylphosphinoylallene derivatives are of interest as potential agonists of nicotinic acetylcholine neuroreceptors (nAChRs)
合成了具有ClCH 2基团的
二苯基膦酰基烯
丙二烯,并研究了它们与胱
氨酸的反应。结果表明,该反应涉及排他性的是
氯甲基中
氯的亲核取代。胱
氨酸与
二苯基膦酰基烯
丙二烯衍
生物的合成缀合物作为
烟碱型
乙酰胆碱神经受体(nAChRs)的潜在激动剂是令人感兴趣的。