吲哚分子间不对称去芳构化氧化Heck反应  

Intermolecular Enantioselective Dearomative Oxidative Heck Reaction of Indoles

作　　者：高炜洋 邓伟超 高扬 梁仁校[1] 贾义霞[1] Gao Weiyang;Deng Weichao;Gao Yang;Liang Renxiao;Jia Yixia(College of Chemical Engineering,Zhejiang University of Technology,Hangzhou 310014)

机构地区：[1]浙江工业大学化学工程学院,杭州310014

出　　处：《化学学报》2024年第1期1-4,共4页Acta Chimica Sinica

基　　金：国家自然科学基金(Nos.22371255,22371254,22071217)资助。

摘　　要：过渡金属催化的不对称去芳构化反应是合成手性环状化合物的直接方法之一.近年来,基于Heck反应已成功实现吲哚、苯并呋喃、吡咯、呋喃及萘等芳香化合物的不对称去芳构化反应.然而,现有报道往往局限于分子内反应,分子间不对称去芳构化Heck反应仍有待研究.与Heck反应相比,氧化Heck反应由于反应条件相对温和且可能经历离子型催化机理,利于实现分子间去芳构化反应并控制其对映选择性.本工作发展了钯催化吲哚与芳基硼酸的分子间不对称去芳构化氧化Heck反应.以Pd(OAc)2为催化剂前体、吡啶-噁唑啉为手性配体、苯醌-氧气为氧化剂,以中等至良好的收率及中等水平的ee值,合成了一系列含有C2-季碳手性中心的手性吲哚啉衍生物.Transition-metal-catalyzed asymmetric dearomatization reaction represents a straightforward method to access chiral cyclic compounds.In recent years,enantioselective dearomative Heck reactions of indoles,benzofurans,pyrroles,furans,and naphthalenes have been successfully developed.Nevertheless,current reports are mainly limited to the intramolecular reaction,the intermolecular asymmetric dearomative Heck reactions are still underdeveloped.In consideration of the relatively mild reaction conditions in oxidative Heck reaction,we envisioned that the intermolecular dearomative oxidative Heck reaction and its asymmetric induction might be possible due to its commonly-proposed cationic rather than neutral mechanism for Heck reaction.In the present work,an enantioselective palladium-catalyzed intermolecular dearomative Heck reaction of indoles with arylboronic acids has been developed.By employing Pd(OAc)2 as the catalyst precursor,pyridineoxazoline as the chiral ligand,oxygen as an oxidant,and benzoquinone(BQ) as the co-oxidant,a series of chiral indolines bearing a C2-substituted quaternary stereocenter were afforded in moderate to good yields and moderate ee values.A general procedure for this enantioselective dearomative oxidative Heck reaction is described as the following:To a dried Schlenk tube were charged with Pd(OAc)2(4.5 mg,10 mol%) and ligand L9(15.1 mg,20 mol%) under O2 atmosphere.2 mL of N-methylpyrrolidone(NMP) solvent was then introduced via a syringe and the Schlenk tube was sealed using a Teflon cap.The mixture was stirred at 60 ℃ for 30 min in order to form the catalyst complex.After cooling to room temperature,indole substrates 1(0.2 mmol),aryl boronic acids(0.6 mmol),and co-oxidant BQ(4.3 mg,20 mol%) were added to the reaction system under O2 atmosphere.The resulting mixture was then stirred at 80 ℃ for 12 h.When the reaction was completed [monitored by thin-layer chromatography(TLC)],10 mL of water was added to the reaction system and the mixture was extracted with ethyl acetate.The combined or

关 键 词：氧化Heck反应 吲哚 分子间 去芳构化 手性吲哚啉 

分 类 号：O621.251[理学—有机化学]