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Enantiospecific and Iterative Suzuki-Miyaura Cross-Couplings

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 139, Issue 50, Pages 18124-18137

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.7b08326

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Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canada Foundation for Innovation (CFI)
  3. Ontario Government
  4. Queen's University
  5. Grants-in-Aid for Scientific Research [16K13962, 17H03030, 26288023] Funding Source: KAKEN

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The Suzuki-Miyaura cross-coupling reaction has emerged as one of the most powerful methods for the construction of carbon-carbon bonds. Though most widely utilized for the synthesis of sp(2)-sp(2) linkages, the use of this reaction to form stereochemistry-bearing sp(2)-sp(3) bonds has received widespread attention over the past decade. This Perspective highlights approaches to the synthesis of enantioenriched molecules via the Suzuki-Miyaura reaction. Particular focus is placed on the use of enantiomerically enriched organoboron compounds as coupling partners in stereospecific processes, as well as the development of enantioconvergent and group-selective reactions. In addition, progress in the development of chemoselective, iterative cross-coupling methods will be discussed.

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