target compounds were generated via the formation of β-enamino diketone as a key intermediate, followed by intramolecular Diels–Alder cycloaddition. The prepared molecules bearing a quinoline-2,4-dione moiety could be further brominated with N-bromosuccinimide and diastereoselectively reduced by NaBH4 to afford pyrano[3,2-c]quinolin-5-one-derived heterocycles with six vicinal stereogenic centers.
通过1,4-二氮杂
双环[2.2.2]辛烷催化、CH 3 NO 2介导的 1,3 三组分反应合成了一系列 1,3-环二酮和四氢环氧异
吲哚稠合的 β-烯
氨基二羰基杂环。 -环二酮、
糠醛和
烯丙胺的
甲苯溶液。目标化合物是通过形成 β-烯
氨基二酮作为关键中间体,然后进行分子内 Diels-Alder 环加成反应生成的。制备的带有 quinoline-2,4-dione 部分的分子可以进一步用N-
溴代琥珀
酰亚胺溴化并被 NaBH 4非对映选择性还原得到
吡喃[3,2- c]quinolin-5-one 衍生的杂环,具有六个邻位立体中心。