We acknowledge funding from the Royal Society (MDS), GSK and the EPSRC (E.E.M. and S.T.), the University of Oxford John Fell Fund and AstraZeneca. We thank Dr. John Ward (GSK) and Dr. Andrew Cridland (GSK) for useful discussions, Dr. Amber Thompson for assistance with X-ray crystallography, and Prof. Ian Fleming FRS for insightful comments.
Catalytic Asymmetric 6π Electrocyclization: Enantioselective Synthesis of Functionalized Indolines†
Article first published online: 4 NOV 2009
Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Volume 121, Issue 52, pages 10164–10167, December 21, 2009
How to Cite
Maciver, Eleanor E., Thompson, S. and Smith, Martin D. (2009), Catalytic Asymmetric 6π Electrocyclization: Enantioselective Synthesis of Functionalized Indolines. Angew. Chem., 121: 10164–10167. doi: 10.1002/ange.200905169
- Issue published online: 15 DEC 2009
- Article first published online: 4 NOV 2009
- Manuscript Received: 15 SEP 2009
- Royal Society
- University of Oxford John Fell Fund
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