4.4 Article

Direct Amination of Phenols under Metal-Free Conditions

Journal

SYNLETT
Volume 24, Issue 11, Pages 1448-1454

Publisher

GEORG THIEME VERLAG KG
DOI: 10.1055/s-0033-1338703

Keywords

amination; phenols; metal-free; arylamines; carbazoles

Funding

  1. National Natural Science Foundation of China [31071720]

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Herein, we disclose the metal-free synthesis of arylamines via the direct amination of phenols using aminating reagents. This reaction procedure uses easy accessible aminating reagents and provides a versatile synthetic route to a broad range of arylamines with various functionalities in good to excellent yield. By using a two-step route of amination and oxidative coupling reaction, we synthesized three naturally occurring carbazole alkaloids: murrayafoline A, mukonine, and clausenine from two commercially available phenols.

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