Enantioselective synthesis and selective functionalization of 4‐aminotetrahydroquinolines as novel GLP‐1 secretagogues
作者:Mustafa Z. Kazancioglu、Kevin Quirion、Peter Wipf、Erin M. Skoda
DOI:10.1002/chir.23403
日期:2022.3
obtained in moderate to high yields (28% to 92%) and enantiomeric ratios (er 89:11 to 99:1) by a three-component Povarov reaction using a chiral phosphoric acid catalyst. Significantly, post-Povarov functional group interconversions allowed a rapid access to a library of 36 enantioenriched 4-aminotetrahydroquinoline derivatives featuring five points of diversity. Selected analogs were assayed for their
通过使用手性磷酸催化剂的三组分 Povarov 反应,以中高产率(28% 至 92%)和对映体比(er 89:11 至 99:1)获得多取代四氢喹啉。值得注意的是,后 Povarov 官能团相互转换允许快速访问具有 5 个多样性点的 36 种对映体富集 4-氨基四氢喹啉衍生物的库。对选定的类似物进行了测定,以确定它们作为胰高血糖素样肽-1 (GLP-1) 促分泌素发挥作用的能力。