Gore Babasaheb Sopan, Chen Chun-Cheng, Lin Ping-Yu, Wang Jeh-Jeng
Department of Medicinal and Applied Chemistry, Kaohsiung Medical University, No. 100, Shih-Chuan First Rd, Sanmin District, Kaohsiung City 807, Taiwan.
Department of Medical Research, Kaohsiung Medical University Hospital, No. 100, Tzyou First Rd, Sanmin District, Kaohsiung City 807, Taiwan.
Org Lett. 2024 Jan 26;26(3):757-762. doi: 10.1021/acs.orglett.3c04246. Epub 2024 Jan 17.
A dual nickel- and iridium-photocatalyzed radical cascade bicyclization reaction for the synthesis of highly complex molecular structures in an atom- and step-economic manner has been described. A series of radical precursors are utilized for the divergent synthesis of diversely substituted fluorenes and indenoazepinones bearing quaternary carbons by using cascade cyclization reactions of 1,5-enynes. This reaction is characterized by its mild conditions, broad substrate scope, excellent selectivity, and satisfactory yield including facile scale-up synthesis.
已报道了一种双镍和铱光催化自由基串联双环化反应,该反应以原子经济性和步骤经济性的方式合成高度复杂的分子结构。通过1,5-烯炔的串联环化反应,一系列自由基前体被用于不同取代的含季碳芴和茚并氮杂卓酮的发散合成。该反应具有条件温和、底物范围广、选择性优异以及收率令人满意等特点,包括易于放大合成。