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- W2022022083 endingPage "11055" @default.
- W2022022083 startingPage "11034" @default.
- W2022022083 abstract "In this Article, a strategy to obtain highly enantioselective catalysts for the Claisen rearrangement of allyloxy- and propargyloxy-indoles is outlined. Ultimately, copper BOX and palladium BINAP or PHOX catalysts were discovered as superior in catalyzing Claisen rearrangements of allyloxy- or proparyloxy-substituted indoles to generate oxindoles bearing allyl- or allenyl-substituted quaternary centers. This method proved to be tolerant of a broad range of functional groups. Tandem reactions of the silyl-allene products provide rapid access to a variety of spirocyclic oxindoles in one operation." @default.
- W2022022083 created "2016-06-24" @default.
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- W2022022083 creator A5052701906 @default.
- W2022022083 creator A5072730133 @default.
- W2022022083 creator A5086746388 @default.
- W2022022083 date "2012-12-04" @default.
- W2022022083 modified "2023-10-16" @default.
- W2022022083 title "Copper(II)- and Palladium(II)-Catalyzed Enantioselective Claisen Rearrangement of Allyloxy- and Propargyloxy-Indoles to Quaternary Oxindoles and Spirocyclic Lactones" @default.
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