An efficient amino acid-/self-/base-/ruthenium-/thermal-catalyzed two-step process for the synthesis of functionalized drug-like carbocycles was achieved through combinations of cascade TCRA/C-allylation/enyne-RCM/Diels–Alder reactions as key steps starting from simple acyclic substrates. In this communication, we report the two-step synthesis of drug-like carbocycles through a combination of organocatalysis with ruthenium-catalysis.
通过将级联的TCRA/C-烯丙基化/烯炔-环化/狄尔斯-阿尔德反应作为关键步骤,从简单的非环状底物出发,成功实现了一种高效的
氨基酸/自催化/碱性/
钌/热催化的两步合成功能化药物类碳环的过程。在本次交流中,我们报告了通过将有机催化与
钌催化结合进行药物类碳环的两步合成。