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作 者:Qiao Song Yan Liu Linlin Cai Xinyu Cao Shan Qian Zhouyu Wang
机构地区:[1]Department of Pharmaceutics Engineering,Xihua University,Chengdu 610039,China [2]Department of Chemistry,Xihua University,Chengdu 610039,China
出 处:《Chinese Chemical Letters》2022年第4期2212-2212,共1页中国化学快报(英文版)
摘 要:The authors regret that an interesting work about amide activation left uncited in the above-titled publication.An corrigendum is given as follows:In 2017,Huang’s group[1]reported an interesting method consisting of the amide activation(Tf_(2)0)induced dehydracoupling of halo-genated secondary amides with alkenes and NaBH4 reduction triggered tandem cyclization reaction.It is an efficient strategy to construct substituted pyrrolidine,piperidine,indolizidine,quinolizidine ring systems,and enimino carbocycles.
关 键 词:reaction activation FUSED
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