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• W4245808250 abstract "So selektiv: Die effiziente Titelreaktion umfasst die Palladium(0)-katalysierte Insertion einer CC-Bindung in eine benzylische C(sp3)-H-Bindung; dadurch entstehen 2-Methylen-2,3-dihydrobenzofurane, die bei Behandlung mit einer schwachen Säure (z. B. Essigsäure) und Elektrophilen in Benzofurane übergehen. Die Alkinoxygruppe wirkt dabei als dirigierende Gruppe und erleichtert die C-H-Funktionalisierung. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article." @default.
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• W4245808250 date "2013-08-16" @default.
• W4245808250 modified "2023-10-14" @default.
• W4245808250 title "Palladium-Catalyzed Hydrobenzylation of<i>ortho</i>-Tolyl Alkynyl Ethers by Benzylic CH Activation: Remarkable Alkynoxy-Directing Effect" @default.
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• W4245808250 doi "https://doi.org/10.1002/ange.201304893" @default.
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