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• W2959134429 startingPage "1436" @default.
• W2959134429 abstract "Abstract The 3‐fluorooxindole and tetrahydroisoquinoline scaffolds are both important structures because of their associated biological and pharmaceutical activities. Herein, we report a highly diastereoselective synthesis of 3‐fluorooxindoles fully substituted at the 3‐position and containing a tetrahydroisoquinoline fragment, through the visible‐light photoredox‐catalyzed cross‐dehydrogenative coupling of tetrahydroisoquinolines with 3‐fluorooxindoles. The protocol featured a wide substrate scope: N‐alkyl‐, N‐haloalkyl‐, N‐aryl‐, N‐allyl‐, N‐propargyl‐, and NH 3‐fluorooxinloles were all able to be used to form the desired coupling products in up to 92% yield and 99 : 1 anti/syn ." @default.
• W2959134429 created "2019-07-23" @default.
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• W2959134429 date "2019-07-26" @default.
• W2959134429 modified "2023-09-27" @default.
• W2959134429 title "Visible‐Light Photoredox‐Catalyzed Cross‐Dehydrogenative Coupling of Tetrahydroisoquinolines with 3‐Fluorooxindoles" @default.
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• W2959134429 doi "https://doi.org/10.1002/ajoc.201900378" @default.
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