4.2 Article

VISIBLE-LIGHT-PROMOTED Se-ARYLATION OF DIARYL DISELENIDES WITH 2-PHENYLIMIDAZOPYRIDINES IN THE PRESENCE OF AMMONIUM IODIDE: SYNTHESIS OF 2-PHENYL-3-(ARYLSELANYL)IMIDAZO[1,2-a]PYRIDINES

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HETEROCYCLES
卷 99, 期 1, 页码 596-603

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.3987/COM-18-S(F)3

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  1. Institute of Pharmaceutical Life Sciences, Aichi Gakuin University
  2. Hokuriku University

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Photoreaction of diaryl diselenides and 2-phenylimidazo[1,2-a]pyridine in the presence of ammonium iodide (20 mol%) using blue LED light led to the formation of 3-(arylselanyl)imidazopyridines in good-to-excellent yields under aerobic conditions. By using various diselenides, this reaction efficiently introduces the selanyl group at the 3-position of the imidazopyridine scaffold.

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