4.8 Article

Organophotoredox-Catalyzed C(sp2)-H Difluoromethylenephosphonation of Imidazoheterocycles

Journal

ORGANIC LETTERS
Volume 21, Issue 14, Pages 5606-5610

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.9b01954

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Funding

  1. CSIR, New Delhi [02(0307)/17/EMR-II]
  2. UGC-New Delhi (UGC-SRF)
  3. CSIR-New Delhi (CSIR-SRF)

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A mild and efficient method for the direct difluoromethylenephosphonation of imidazopyridines has been developed using rose bengal (RB) as a photoredox catalyst. Bis(pinacolato)diboron (B(2)pin(2)) is found to be a crucial additive in the present reaction. The present methodology is also applicable to other heterocycles like imidazo[2,1-b]thiazole, benzo[d]imidazo-[2,1-b]thiazole, and indole. The reaction possibly proceeds through a single electron transfer (SET) process.

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