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- W2223386351 endingPage "177" @default.
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- W2223386351 abstract "Abstract An efficient, chemoselective approach to spiro‐epoxyoxindoles via the addition of chloromethyllithium followed by ring‐closure of the intermediate alkoxide is reported. Chemoselectivity is fully preserved in the presence of different electrophilic sites. The synthetic potential of selected spiro‐epoxyindoles has been exploited in the copper(I)‐catalyzed intramolecular oxyarylation of an alkyne and in the formation of N,N ‐dimethylisoindigo via the addition of dihalocarbenoids. magnified image" @default.
- W2223386351 created "2016-06-24" @default.
- W2223386351 creator A5007946582 @default.
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- W2223386351 creator A5022361290 @default.
- W2223386351 creator A5028086517 @default.
- W2223386351 creator A5059295485 @default.
- W2223386351 date "2016-01-05" @default.
- W2223386351 modified "2023-10-07" @default.
- W2223386351 title "Chemoselective Addition of Halomethyllithiums to Functionalized Isatins:A Straightforward Access to Spiro‐Epoxyoxindoles" @default.
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- W2223386351 doi "https://doi.org/10.1002/adsc.201500840" @default.
- W2223386351 hasPublicationYear "2016" @default.