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Photoinduced Trifluoromethylation with CF3Br as a Trifluoromethyl Source: Synthesis of α-CF3-Substituted Ketones.


ABSTRACT: An efficient and novel photoinduced trifluoromethylation employing CF3Br as a trifluoromethyl source is described. With commercially accessible fac-Ir(III)(ppy)3 as the catalyst, radical trifluoromethylation between O-silyl enol ether and CF3Br occurs successfully. This method provides various α-CF3-substituted ketones with a broad substrate scope in good yields under mild reaction conditions.

SUBMITTER: Ma R 

PROVIDER: S-EPMC9089747 | biostudies-literature | 2022 Apr

REPOSITORIES: biostudies-literature

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Photoinduced Trifluoromethylation with CF<sub>3</sub>Br as a Trifluoromethyl Source: Synthesis of α-CF<sub>3</sub>-Substituted Ketones.

Ma Ransong R   Deng Zhoubin Z   Wang Ke-Hu KH   Wang Junjiao J   Huang Danfeng D   Su Yingpeng Y   Hu Yulai Y   Lv Xiaobo X  

ACS omega 20220412 16


An efficient and novel photoinduced trifluoromethylation employing CF<sub>3</sub>Br as a trifluoromethyl source is described. With commercially accessible <i>fac</i>-Ir<sup>(III)</sup>(ppy)<sub>3</sub> as the catalyst, radical trifluoromethylation between <i>O</i>-silyl enol ether and CF<sub>3</sub>Br occurs successfully. This method provides various α-CF<sub>3</sub>-substituted ketones with a broad substrate scope in good yields under mild reaction conditions. ...[more]

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