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Phosphine-Free Ru-Catalyzed Regio- and Stereoselective Addition of Benzoic Acids to Trifluoromethylated Alkynes toward Facile Access to Trifluoromethyl Group-Substituted (E)-Enol Esters.


ABSTRACT: A combination of ruthenium catalyst with silver salt and copper salt was proved to be a highly efficient protocol for the direct addition reaction of benzoic acids with unsymmetrical trifluoromethylated internal alkynes. Diverse trifluoromethyl group-substituted (E)-enol esters were readily obtained for a broad substrate scope in moderate to good yields with excellent regio- and stereoselectivities under mild reaction conditions.

SUBMITTER: Liu G 

PROVIDER: S-EPMC7057715 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

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Phosphine-Free Ru-Catalyzed Regio- and Stereoselective Addition of Benzoic Acids to Trifluoromethylated Alkynes toward Facile Access to Trifluoromethyl Group-Substituted (<i>E</i>)-Enol Esters.

Liu Guangyuan G   Zhang Xingxing X   Kuang Guanghua G   Lu Naihao N   Fu Yang Y   Peng Yiyuan Y   Xiao Qiang Q   Zhou Yirong Y  

ACS omega 20200220 8


A combination of ruthenium catalyst with silver salt and copper salt was proved to be a highly efficient protocol for the direct addition reaction of benzoic acids with unsymmetrical trifluoromethylated internal alkynes. Diverse trifluoromethyl group-substituted (<i>E</i>)-enol esters were readily obtained for a broad substrate scope in moderate to good yields with excellent regio- and stereoselectivities under mild reaction conditions. ...[more]

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