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- W2144234884 endingPage "2273" @default.
- W2144234884 startingPage "2265" @default.
- W2144234884 abstract "The gold-catalyzed reaction of 2-alkynyl-phenylamines with α,β-enones represents a new general one-pot entry into C-3-alkyl-indoles by sequential reactions. Gold-catalyzed sequential cyclization/alkylation, N-alkylation/cyclization, or N-alkylation/cyclization/alkylation reactions leading to different indoles can be directed by changing the 2-alkynyl-phenylamine 1/α,β-enone 3 ratio and the reaction temperature. Unusual gold-catalyzed rearrangement reaction of indoles are observed at 140 °C. New gold-catalyzed formation of propargyl-alkyl ether under mild conditions and the hydration reaction of N-acetyl-2-ethynyl-phenylamine are reported." @default.
- W2144234884 created "2016-06-24" @default.
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- W2144234884 creator A5085959630 @default.
- W2144234884 date "2005-02-19" @default.
- W2144234884 modified "2023-10-11" @default.
- W2144234884 title "Gold-Catalyzed Reactions of 2-Alkynyl-phenylamines with α,β-Enones" @default.
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