Chinese Journal of Organic Chemistry >
Visible-Light Promoted Preparation of Trifluoromethylated Tetrahydrofuran and Tetrahydropyran
Received date: 2018-08-31
Revised date: 2018-09-26
Online published: 2018-10-20
Supported by
Project supported by the National Natural Science Foundation of China (Nos. 21722203, 21831002, 21801116, and 21572096), the Shenzhen Special Funds for the Development of Biomedicine, Internet, New Energy, and New Material Industries (Nos. JCYJ20170412152435366, JCYJ20170307105638498), the Natural Science Foundation of Guangdong Province (No. 2018A030310083) and the Shenzhen Nobel Prize Scientists Laboratory Project (No. C17213101).
An efficient protocol for facile access to trifluoromethylated tetrahydrofuran and tetrahydropyran has been developed under visible light irradiation conditions via radical 1,2-alkoxyl-trifluoromethylation of unactivated alkene. It features the use of readily commercially available and operatively simple trifluoromethanesulfonyl chloride as a trifluoro- methyl radical source, thus making the protocol potentially appealing for practical preparation.
Wang Na , Gu Qiang-Shuai , Cheng Yong-Feng , Li Lei , Li Zhong-Liang , Guo Zhen , Liu Xin-Yuan . Visible-Light Promoted Preparation of Trifluoromethylated Tetrahydrofuran and Tetrahydropyran[J]. Chinese Journal of Organic Chemistry, 2019 , 39(1) : 200 -206 . DOI: 10.6023/cjoc201808048
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