4.8 Article

Palladium-Catalyzed Difunctionalization of Internal Alkynes via Highly Regioselective 6-Endo Cyclization and Alkenylation of Enynoates: Synthesis of Multisubstituted Pyrones

Journal

ORGANIC LETTERS
Volume 17, Issue 7, Pages 1636-1639

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b00272

Keywords

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Funding

  1. National Natural Science Foundation of China [21372210, 21432009]
  2. Natural Science Foundation of Anhui Province [1308085QB37]
  3. National Science Foundation for Postdoctoral Scientists of China [2012M521231]
  4. Nanyang Technology University

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An efficient Pd(II)-catalyzed difunctionalization reaction of internal alkynes is reported. In this reaction, various enynoates and electron-deficient alkenes were used for the syntheses of useful highly substituted pyrone derivatives via a 6-endo cyclization and subsequent alkenylation pathway. The corresponding products could be obtained in moderate to good yields under very mild reaction conditions. The high regioselectivity and wide compatibility with different functional groups found in the desired products demonstrate this method to be a general and useful tool for the synthesis of highly substituted pyrone derivatives.

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