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- W2950373323 abstract "AuCl-catalyzed intramolecular hydroamination of N-aryl-O-propargyl carbamates (3) efficiently affords (Z)-N-aryl-4-benzyliden-2-oxazolidinones (4) via a 5-exo dig cyclization. The reaction proceeds in acetonitrile at 60 °C and requires tBuOK or KOH as a base co-catalyst. It tolerates the presence of multiple substituted aryl units with electron donating methoxy groups. The method opens a convenient, flexible and operationally simple access to a new class of twisted molecules with potentially interesting biological properties." @default.
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- W2950373323 date "2007-01-01" @default.
- W2950373323 modified "2023-09-23" @default.
- W2950373323 title "Synthesis of 4-Benzyliden-2-oxazolidinone Derivatives via Gold-Catalyzed Intramolecular Hydroamination" @default.
- W2950373323 cites W2017662055 @default.
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- W2950373323 doi "https://doi.org/10.3987/com-07-s(w)58" @default.
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