| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1314634 | Journal of Fluorine Chemistry | 2012 | 7 Pages |
A convenient and efficient method for oxidative coupling of tetrahydroisoquinoline derivatives with trimethyl(trifluoromethyl)silane and terminal alkynes to 1-trifluoromethylated or 1-alkynylated tetrahydroisoquinolines via CH activation was developed using visible light irradiation. The protocol uses Rose Bengal as the catalyst, air as terminal oxidant, and the trifluoromethylation or alkynylation was selectively performed at the α-position of nitrogen under extremely mild conditions.
Graphical abstractA convenient and efficient method for oxidative coupling of tetrahydroisoquinoline derivatives with trimethyl(trifluoromethyl)silane and terminal alkynes to 1-trifluoromethylated or 1-alkynylated tetrahydroisoquinolines via CH activation was developed using visible light irradiation. The protocol uses Rose Bengal as the catalyst, air as terminal oxidant, and the trifluoromethylation or alkynylation was selectively performed at the α-position of nitrogen under extremely mild conditions.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Rose Bengal catalyzed α-trifluoromethylation and α-alkynylation of tetrahydroisoquinolines under visible light irradiation. ► The reaction via CH activation. ► The reaction uses air as terminal oxidant under transition-metal-free reaction conditions.
