4.7 Article

Diastereoselective 1,3-Dipolar Cycloaddition of Nitrones to Donor-Acceptor Cyclopropanes Catalyzed by a Calcium(II) Complex

Journal

JOURNAL OF ORGANIC CHEMISTRY
Volume 80, Issue 3, Pages 1979-1984

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jo502686t

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Funding

  1. American Chemical Society Petroleum Research Fund
  2. Arnold and Mabel Beckman Foundation
  3. Thomas F. and Kate Miller Jeffress Trust
  4. University of Richmond

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Calcium triflate has been identified as an efficient catalyst for the cycloaddition of nitrones to donor-acceptor cyclopropanes. The reaction proceeds with good to excellent yields of the corresponding tetrahydro-1,2-oxazines with high levels of diastereoselectivity. The generality of the reaction allowed for the synthesis of tetrahydro-1,2-oxazines bearing alkyl, aryl, and heteroaromatic substitution.

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