4.7 Article

A new dehydrogenative [4+1] annulation between para-quinone methides (p-QMs) and iodonium ylides for the synthesis of 2,3-dihydrobenzofurans

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 5, Issue 23, Pages 3483-3487

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8qo00950c

Keywords

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Funding

  1. NSFC [21472071, 21602087]
  2. Outstanding Youth Fund of JSNU [YQ2015003]
  3. NSF of Jiangsu Province [BK20160212]
  4. Qing Lan Project of Jiangsu Education Committee

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A new dehydrogenative [4 + 1] annulation of para-quinone methides (p-QMs) with acyclic and cyclic phenyl iodonium ylides has been established, delivering a variety of functionalized 2,3-dihydrobenzofurans with the retention of the quinone methide unit in generally good yields. The reaction pathway involves 1,6-nucleophilic addition, nucleophilic substitution and oxidation under mild metal-free and convenient conditions, and provides a practical access to construct benzofuran frameworks.

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