We thank the National Institutes of Health (R01GM033049) and the National Science Foundation for their generous support of our programs. J.T.M. is supported by an Abbott Laboratories Stanford Graduate Fellowship. We also thank Johnson-Matthey for their generous gift of palladium salts.
Palladium-Catalyzed Asymmetric Allylic Alkylation of 3-Aryloxindoles with Allylidene Dipivalate: A Useful Enol Pivalate Product†
Article first published online: 17 JAN 2013
Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Angewandte Chemie International Edition
Volume 52, Issue 8, pages 2260–2264, February 18, 2013
How to Cite
Trost, B. M., Masters, J. T. and Burns, A. C. (2013), Palladium-Catalyzed Asymmetric Allylic Alkylation of 3-Aryloxindoles with Allylidene Dipivalate: A Useful Enol Pivalate Product . Angew. Chem. Int. Ed., 52: 2260–2264. doi: 10.1002/anie.201209783
- Issue published online: 13 FEB 2013
- Article first published online: 17 JAN 2013
- Manuscript Received: 7 DEC 2012
- National Institutes of Health. Grant Number: R01GM033049
- National Science Foundation
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