4.8 Article

Nickel-Catalyzed Double Carboxylation of Alkynes Employing Carbon Dioxide

Journal

ORGANIC LETTERS
Volume 16, Issue 18, Pages 4960-4963

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol502538r

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Funding

  1. MEXT, Japan [22000009]
  2. JSPS [25708017]
  3. Grants-in-Aid for Scientific Research [25708017, 14J00435] Funding Source: KAKEN

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The nickel-catalyzed double carboxylation of internal allcynes employing carbon dioxide (CO2) has been developed. The reactions proceed under CO2 (1 atm) at room temperature in the presence of a nickel catalyst, Zn powder as a reducing reagent, and MgBr2 as an indispensable additive. Various internal alkynes could be converted to the corresponding maleic anhydrides in good to high yields. DFT calculations disclosed the indispensable role of MgBr2 in the second CO2 insertion.

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