We sincerely thank the National Institutes of Health (GM54623) for generous financial support. We also thank Johnson and Johnson for a Focused Giving Award, Pfizer Pharmaceuticals for the Creativity in Organic Chemistry Award, and Novartis Pharmaceuticals for an Academic Achievement Award. The Camille and Henry Dreyfus Foundation is thanked for a Camille Dreyfus Teacher-Scholar Award (P.A.E.).
Diastereoselective Temporary Silicon-Tethered Ring-Closing-Metathesis Reactions with Prochiral Alcohols: A New Approach to Long-Range Asymmetric Induction†
Version of Record online: 16 APR 2003
© 2002 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Angewandte Chemie International Edition
Volume 42, Issue 15, pages 1734–1737, April 17, 2003
How to Cite
Evans, P. A., Cui, J. and Buffone, G. P. (2003), Diastereoselective Temporary Silicon-Tethered Ring-Closing-Metathesis Reactions with Prochiral Alcohols: A New Approach to Long-Range Asymmetric Induction. Angew. Chem. Int. Ed., 42: 1734–1737. doi: 10.1002/anie.200250486
- Issue online: 16 APR 2003
- Version of Record online: 16 APR 2003
- Manuscript Received: 6 NOV 2002
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