4.8 Article

Photocatalytic Asymmetric Epoxidation of Terminal Olefins Using Water as an Oxygen Source in the Presence of a Mononuclear Non-Heme Chiral Manganese Complex

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 138, Issue 49, Pages 15857-15860

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.6b10836

Keywords

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Funding

  1. NRF of Korea through the CRI Program [NRF-2012R1A3A2048842]
  2. NRF of Korea through the GRL Program [NRF-2010-00353]
  3. JSPS KAKENHI [16H02268]
  4. National Natural Science Foundation of China [21473226]
  5. National Research Foundation of Korea [NRF-2015H1D3A1066507]
  6. National Research Foundation of Korea [2012R1A3A2048842, 2015H1D3A1066507, 2010-00353] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  7. Grants-in-Aid for Scientific Research [16H02268] Funding Source: KAKEN

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Photocatalytic enantioselective epoxidation of terminal olefins using a mononuclear non-heme chiral manganese catalyst, [(R,R-BQCN)Mn-II](2+), and water as an oxygen source yields epoxides with relatively high enantioselectivities (e.g., up to 60% enantiomeric excess). A synthetic mononuclear non-heme chiral Mn(IV)-oxo complex, [(R,R-BQCN)Mn-IV(O)](2+), affords similar enantioselectivities in the epoxidation of terminal olefins under stoichiometric reaction conditions. Mechanistic details of each individual step of the photoinduced catalysis, including formation of the Mn(IV)-oxo intermediate, are discussed on the basis of combined results of laser flash photolysis and other spectroscopic methods.

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