4.5 Article

Iron-Catalyzed Sulfur-Promoted Decyanative Redox Condensation of o-Nitrophenols and Arylacetonitriles: An Unprecedented Route to 2-Arylbenzoxazoles

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EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
卷 2018, 期 42, 页码 5815-5818

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/ejoc.201701607

关键词

Transition metals; Iron catalysis; redox condensation; benzoxazole; benzyl cyanide

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Elemental sulfur in the presence of a catalytic amount of FeCl2 center dot 4H(2)O was found to be highly efficient for the promotion of decyanative redox condensation reactions of o-nitrophenols with arylacetonitriles, to give a wide range of 2-arylbenzoxazoles. The utility of elemental sulfur was highlighted by its role as cyanide scavenger and external reducing agent.

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