4.7 Article

Unexpected C-C bond cleavage of epoxide motif: Rhodium(I)-catalyzed tandem heterocyclization/[4+1] cycloaddition of 1-(1-alkynyl)oxiranyl ketones

Journal

CHEMICAL COMMUNICATIONS
Volume 47, Issue 19, Pages 5578-5580

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c0cc05650b

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Funding

  1. NSFC [20972054]
  2. Ministry of Education of China
  3. STCSM [08dj1400100]
  4. 973 Program [2009CB825300]

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A rhodium(I)-catalyzed tandem heterocyclization and formal [4+1] cycloaddition of 1-(1-alkynyl)oxiranyl ketones was developed, which provides a general, efficient and practical route to highly substituted furo[3,4-b]furan-3(2H)-ones, wherein the epoxide motif undergo unexpected C-C bond cleavage rather than the classical C-O bond cleavage.

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