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- W4372319329 endingPage "1692" @default.
- W4372319329 startingPage "1685" @default.
- W4372319329 abstract "Abstract Installation of an alkyl chain at a specified position in the aromatic ring via metal‐free catalysis is very important. In this regard, we have developed a facile metal‐free, extremely selective, user‐friendly, environmentally benign and cost‐effective Friedel‐Crafts (FC) alkylation protocol for 2‐oxindoles and anilines with donor‐acceptor cyclopropanes. Real‐time NMR studies reveal that the transformation is governed by the cooperative catalysis of Brønsted acid (TfOH) and HFIP, which facilitates the nucleophilic attack on donor‐acceptor cyclopropanes from 2‐oxindoles and anilines. magnified image" @default.
- W4372319329 created "2023-05-07" @default.
- W4372319329 creator A5004697426 @default.
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- W4372319329 creator A5049440381 @default.
- W4372319329 creator A5058414158 @default.
- W4372319329 date "2023-05-16" @default.
- W4372319329 modified "2023-10-12" @default.
- W4372319329 title "HFIP & Brønsted Acid Promoted Direct Distal <i>C</i>‐Alkylation of 2‐Oxindoles and Anilines with Donor‐Acceptor Cyclopropanes" @default.
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- W4372319329 doi "https://doi.org/10.1002/adsc.202300165" @default.
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