We thank the NSERC, Merck Frosst Canada, and the University of Toronto for support of our programs, Jérémy Ruiz for initial studies using the N-Cbz azabicycle, Alena Rudolph for initial studies into the enantioselective reaction, and Dr. Christopher Dockendorff for first bringing this natural product to our attention.
Enantioselective Total Synthesis of (+)-Homochelidonine by a PdII-Catalyzed Asymmetric Ring-Opening Reaction of a meso-Azabicyclic Alkene with an Aryl Boronic Acid†
Article first published online: 5 DEC 2006
Copyright © 2007 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Volume 119, Issue 3, pages 437–440, January 8, 2007
How to Cite
McManus, Helen A., Fleming, Matthew J. and Lautens, M. (2007), Enantioselective Total Synthesis of (+)-Homochelidonine by a PdII-Catalyzed Asymmetric Ring-Opening Reaction of a meso-Azabicyclic Alkene with an Aryl Boronic Acid. Angew. Chem., 119: 437–440. doi: 10.1002/ange.200603945
- Issue published online: 27 DEC 2006
- Article first published online: 5 DEC 2006
- Manuscript Received: 26 SEP 2006
- Merck Frosst Canada
- University of Toronto
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