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Communication

Rhodium-Catalyzed Enantioselective Nucleophilic Fluorination: Ring Opening of Oxabicyclic Alkenes†

  1. Dr. Jiangtao Zhu‡,
  2. Gavin C. Tsui‡,
  3. Prof. Dr. Mark Lautens*

Article first published online: 4 NOV 2012

DOI: 10.1002/anie.201207356

Issue

Angewandte Chemie International Edition

Angewandte Chemie International Edition

Volume 51, Issue 49, pages 12353–12356, December 3, 2012

Additional Information

How to Cite

Zhu, J., Tsui, G. C. and Lautens, M. (2012), Rhodium-Catalyzed Enantioselective Nucleophilic Fluorination: Ring Opening of Oxabicyclic Alkenes . Angew. Chem. Int. Ed., 51: 12353–12356. doi: 10.1002/anie.201207356

Author Information

  1. Davenport Laboratories, Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON, M5S 3H6 (Canada) http://www.chem.utoronto.ca/staff/ML/

  1. ‡

    These authors contributed equally to this work.

*Davenport Laboratories, Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, ON, M5S 3H6 (Canada) http://www.chem.utoronto.ca/staff/ML/

  1. †

    We gratefully thank the NSERC, Merck Frosst, and Merck for an Industrial Research Chair. We also thank the University of Toronto for support of our program, Dr. Alan Lough (Chemistry Department, University of Toronto) for single-crystal X-ray structure analysis, and Solvias AG for the generous gift of chiral ligands. J.Z. thanks SIOC for a postdoctoral fellowship. G.C.T. thanks NSERC for a postgraduate scholarship.

  2. ‡

    These authors contributed equally to this work.

Publication History

  1. Issue published online: 28 NOV 2012
  2. Article first published online: 4 NOV 2012
  3. Manuscript Received: 12 SEP 2012

Funded by

  • NSERC
  • Merck Frosst
  • University of Toronto

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