4.8 Article

A complementary pair of enantioselective switchable organocatalysts

Journal

CHEMICAL SCIENCE
Volume 8, Issue 10, Pages 7077-7081

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c7sc02462b

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Funding

  1. Engineering and Physical Sciences Research Council (UK)
  2. Royal Society
  3. Engineering and Physical Sciences Research Council [EP/H021620/2] Funding Source: researchfish
  4. EPSRC [EP/H021620/2] Funding Source: UKRI

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A pair of enantioselective switchable bifunctional catalysts are shown to promote a range of conjugate addition reactions in up to 95 : 5 e.r. and 95% conversion. Each catalyst can be switched OFF using conditions that switch the other catalyst ON. Catalyst ON : OFF ratios of up to 98 : 2 and 1 : 99 were achieved, with a ratio of reaction rates of up to 16 : 1 between the ON and OFF states, maintained over complete ON-OFF-ON and OFF-ON-OFF cycles. However, simultaneous operation of the catalyst pair in the same reaction vessel, which in principle could allow product handedness to be switched by simple E-Z isomerisation of the catalyst pair, was unsuccessful. In this first generation complementary pair of enantioselective switchable organocatalysts, the OFF state of one catalyst inhibits the ON state of the other.

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