Mintz Tomer, Liu Lei, Pappo Doron
Department of Chemistry, Ben-Gurion University of the Negev, Beer-Sheva 8410501, Israel.
School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.
Org Lett. 2025 Jan 31;27(4):1078-1083. doi: 10.1021/acs.orglett.5c00050. Epub 2025 Jan 22.
A novel class of bis-8-aryl-isoquinoline () bis-alkylamine iron complexes, Fe()(OTf) and Fe()(OTf) ( = dipyrrolidinyl or = ,'-dimethylcyclohexyl-diamine), for asymmetric oxidation reactions is reported. The scalable divergent synthesis of 8-aryl-3-formylisoquinolines (), the key intermediates in preparing these ligands, enables precise structural and electronic tuning around the metal center. The enantioselective epoxidation and hydroxy carbonylation of conjugated alkenes, mediated by the Fe() catalyst with HO as the oxidant, demonstrates the potential of these redox Fe[N] catalysts in inducing face selection in oxygen transfer transformations.
报道了一类新型的双-8-芳基异喹啉()双烷基胺铁配合物,即Fe()(OTf)和Fe()(OTf)( = 二吡咯烷基或 = ,'-二甲基环己基二胺),用于不对称氧化反应。作为制备这些配体的关键中间体,8-芳基-3-甲酰基异喹啉()的可扩展发散合成能够在金属中心周围进行精确的结构和电子调节。以HO为氧化剂,由Fe()催化剂介导的共轭烯烃的对映选择性环氧化和羟基羰基化反应,证明了这些氧化还原Fe[N]催化剂在氧转移转化中诱导面选择的潜力。