4.8 Article

2-Methylenetetrahydropyrans: Efficient Partners in the Carbonyl Ene Reaction

Journal

ORGANIC LETTERS
Volume 15, Issue 23, Pages 5974-5977

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol402843s

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Funding

  1. National Institutes of Health [R01 GM064357]
  2. National Science Foundation [CHE 1112370]

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The carbonyl ene reaction of 2-methylenetetrahydropyrans provides a rapid, high yielding route for the preparation of beta-hydroxydihydropyrans under mild conditions. This process provides a new entry for the synthesis of 2-substituted tetrahydropyrans and for the direct introduction of oxygen heterocycles into molecular frameworks.

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