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CuBr-Promoted Tandem Cyclization/Trifluoromethylation of 2-Alkynylanilines: Efficient Synthesis of 3-Trifluoromethylindoles

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摘要 A new efficient strategy for the synthesis of 3-trifluoromethyl-indoles was developed through tandem cyclization/trifluoromethylation of 2-alkynylanilines and Umemoto's reagent under effect of CuBr.The reaction features the use of cheap copper salt,mild reaction conditions and high yield of products.The preliminary mechanism study indicates the solvent dimethylacetamide acts as the role of dealkylation.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2014年第8期727-733,共7页 中国化学(英文版)
基金 Financially supported by the Major Basic Research Development Program(No.2011CB808706) National Natural Science Foundation of China(Nos.21272251,21121062 and 21032007) Chinese Academy of Sciences,the Technology Commission of Shanghai Municipality,and the Croucher Foundation of Hong Kong.
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