Metal-Free Etherification of Aryl Methyl Ether Derivatives by C–OMe Bond Cleavage
A general and efficient protocol was developed for the synthesis of aryl alkyl ethers through metal-free C–OMe bond cleavage under mild reaction conditions. This process displays a wide scope of methoxyarenes and alcohols, including primary, secondary, and tertiary alcohols, as well as natural produ...
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Veröffentlicht in: | Organic letters 2018-07, Vol.20 (14), p.4267-4272 |
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Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | A general and efficient protocol was developed for the synthesis of aryl alkyl ethers through metal-free C–OMe bond cleavage under mild reaction conditions. This process displays a wide scope of methoxyarenes and alcohols, including primary, secondary, and tertiary alcohols, as well as natural products, pharmaceuticals, and biologically active alcohols. DFT calculations and experimental results simultaneously confirm that a potassium ion plays a critical role in the activation of methoxy group via binding with the nitrile and provide support for an SNAr mechanism. |
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ISSN: | 1523-7060 1523-7052 |
DOI: | 10.1021/acs.orglett.8b01696 |