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作 者:Lesong Li Tao Liu Weiwu Ren Yang Wang
机构地区:[1]Molecular Synthesis Center&Key Laboratory of Marine Drugs,Chinese Ministry of Education,School of Medicine and Pharmacy,Ocean University of China,Qingdao 266003,China [2]Laboratory for Marine Drugs and Bioproducts,Qingdao National Laboratory for Marine Science and Technology(QNLM),Qingdao 266237,China
出 处:《Green Synthesis and Catalysis》2024年第1期57-61,共5页绿色合成与催化(英文)
基 金:We thank the Marine S&T Fund of Shandong Province for Pilot National Laboratory for Marine Science and Technology(QNLM)(No.2022QNLM030003-2);the Fundamental Research Funds for the Central Universities,Ocean University of China,Qingdao National Laboratory for Marine Science and Technology(Nos.LMDBCXRC201902 and LMDBCXRC201903);Taishan Scholar Program of Shandong Province(Nos.tsqn201909056 and tsqn202103152);National Natural Science Foundation of China(No.22171251);Natural Science Foundation of Shandong Province(No.ZR2021QB033)for financial support.
摘 要:A catalyst-free and atom-economical[4+3]cycloaddition of azadienes with C,N-cyclic azomethine imines has been developed,providing an efficient and environmentally benign access to 1,2,4-triazepines with high diastereoselectivities and yields.This reaction can be performed in 2-methyltetrahydrofuran under mild conditions smoothly.
关 键 词:CATALYST-FREE Atom-economical[4+3] Cycloaddition C N-cyclic Azomethine imine Azadiene 1 2 4-triazepine
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