Enantioselective assembly of the benzo[d]xanthene tetracyclic core of anti-influenza active natural products.

نویسندگان

  • Ngoc Duc Tran
  • Martin Albicker
  • Lorenz Schneider
  • Nicolai Cramer
چکیده

A combination of an enantioselective conjugate addition/trapping sequence and a ruthenium(iii)-catalyzed domino cyclization provides a concise access to benzo[d]xanthenes found in several anti-influenza active sesquiterpene natural products.

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Enantioselective, convergent synthesis of the ineleganolide core by a tandem annulation cascade† †Electronic supplementary information (ESI) available: Experimental procedures, 1H NMR, 13C NMR, and IR spectra, X-ray crystallographic data. CCDC 853379, 1061009–1061014 and 1061016. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc03347d Click here for additional data file. Click here for additional data file.

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عنوان ژورنال:
  • Organic & biomolecular chemistry

دوره 8 8  شماره 

صفحات  -

تاریخ انتشار 2010