4.8 Article

Visible Light Activation of Boronic Esters Enables Efficient Photoredox C(sp2)-C(sp3) Cross-Couplings in Flow

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 55, Issue 45, Pages 14085-14089

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201605548

Keywords

boronic esters; cross-coupling; flow chemistry; photoredox catalysis; synthetic methods

Funding

  1. Novartis Pharma AG
  2. EPSRC [EP/K0099494/1, EP/K039520/1]
  3. EPSRC [EP/K009494/1, EP/K039520/1] Funding Source: UKRI
  4. Engineering and Physical Sciences Research Council [EP/K009494/1, EP/K039520/1] Funding Source: researchfish

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We report herein a new method for the photoredox activation of boronic esters. Using these reagents, an efficient and high-throughput continuous flow process was developed to perform a dual iridium- and nickel-catalyzed C(sp(2))-C(sp(3)) coupling by circumventing solubility issues associated with potassium trifluoroborate salts. Formation of an adduct with a pyridine-derived Lewis base was found to be essential for the photoredox activation of the boronic esters. Based on these results we were able to develop a further simplified visible light mediated C(sp(2))-C(sp(3)) coupling method using boronic esters and cyano heteroarenes under flow conditions.

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