4.8 Article

Iridium-catalysed direct C-C coupling of methanol and allenes

Journal

NATURE CHEMISTRY
Volume 3, Issue 4, Pages 287-290

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/NCHEM.1001

Keywords

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Funding

  1. Robert A. Welch Foundation [F-0038]
  2. Texas Higher Education Coordinating Board [01849]
  3. University of Texas Center for Green Chemistry and Catalysis
  4. National Science Foundation [CHE-1021640]
  5. Natural Sciences and Engineering Research Council of Canada
  6. German Research Foundation
  7. Direct For Mathematical & Physical Scien
  8. Division Of Chemistry [1021640] Funding Source: National Science Foundation

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Methanol is an abundant (35 million metric tons per year), renewable chemical feedstock, yet its use as a one-carbon building block in fine chemical synthesis is highly underdeveloped. Using a homogeneous iridium catalyst developed in our laboratory, methanol engages in a direct C-C coupling with allenes to furnish higher alcohols that incorporate all-carbon quaternary centres, free of stoichiometric by-products. A catalytic mechanism that involves turnover-limiting methanol oxidation, a consequence of the high energetic demand of methanol dehydrogenation, is corroborated through a series of competition kinetics experiments. This process represents the first catalytic C-C coupling of methanol to provide discrete products of hydrohydroxymethylation.

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