4.8 Article

Transformation of Reactive Isochromenylium Intermediates to Stable Salts and Their Cascade Reactions with Olefins

Journal

ORGANIC LETTERS
Volume 11, Issue 20, Pages 4676-4679

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol9019524

Keywords

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Funding

  1. MOST [2010CB832200, 2009ZX09501]
  2. NSFC [20672128, 20621062]
  3. CAS [KJCX2-YW-H08]
  4. SHMCST [08JC1422800, 07DZ22001]

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Transformation of reactive isochromenylium intermediates to the corresponding storable and stable reagents has been achieved, and a number of isochromerylium tetrafluoroborates (ICTBs, 1) have been conveniently prepared and characterized. Direct metal-free treatment of isochromenylium tetrafluoroborate la with olefins afforded a variety of polycyclic frameworks 4 via mild cascade reactions. Starting from the prefunctionalized o-alkynylbenzaldehydes, a one-pot metal-free procedure of intramolecular cascade annulation to 2,3-dihydrophenanthren-4(1H)-one derivatives was also developed.

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