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作 者:Jun Pan Ziyao Zhang Lili Chen Ning Jiao
机构地区:[1]State Key Laboratory of Natural and Biomimetic Drugs,Chemical Biology Center,Schoolof Pharmaceutical Sciences,Peking University XueYuanRd.38,Beijing 100191,China [2]Shanghai Key Laboratory of Green Chemistry and Chemical Processes,East China Normal University,Shanghai 200062,China
出 处:《Chinese Journal of Chemistry》2023年第5期509-513,共5页中国化学(英文版)
基 金:We acknowledge the National Key R&D Program of China(No.2021YFA1501700);the NSFC(Nos.22131002,22161142019,81821004);the Tencent Foundation for financial support.
摘 要:A rhodium-catalyzed denitrogenative carbonylation of 1,2,3-thiadiazole with alkynes to construct(benzo)thiochromenones is developed.Both terminal and internal alkynes were compatible in this[3+2+1]cycloaddition,affording a broad range of poly-substituted thiochromenones.Unsymmetrical alkyne substrates exhibited good regioselectivity.
关 键 词:Rh-catalysis Transannulation THIADIAZOLES ALKYNES Thiochromenones
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