Journal
ORGANIC LETTERS
Volume 15, Issue 20, Pages 5238-5241Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol402435c
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In situ generated iron sulfide from elemental sulfur and ferric chloride was found to be a highly efficient catalyst for the redox condensation cascade reaction between o-nitroanilines and 2-arylethylamines. This method constitutes a new atom-, step-, and redox-economical route to 2-arylquinoxalines.
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