We thank Dr. Richard I. McDonald and Chun Pong Tam for initiating the synthesis of substrate probe 6-D-1, and Paul B. White and Dr. Charlie G. Fry for assistance with NMR spectroscopic measurements. We thank the NIH (R01 GM67163) and Organic Syntheses (ACS Division of Organic Chemistry fellowship for A.B.W.) for financial support of this work. Spectroscopic instrumentation was partially funded by the NSF (CHE-0342998, CHE-9629688, CHE-9208463) and NIH (1 S10 RR13866-01).
Reconciling the Stereochemical Course of Nucleopalladation with the Development of Enantioselective Wacker-Type Cyclizations†
Article first published online: 16 OCT 2012
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Angewandte Chemie International Edition
Volume 51, Issue 46, pages 11505–11509, November 12, 2012
How to Cite
Weinstein, A. B. and Stahl, S. S. (2012), Reconciling the Stereochemical Course of Nucleopalladation with the Development of Enantioselective Wacker-Type Cyclizations . Angew. Chem. Int. Ed., 51: 11505–11509. doi: 10.1002/anie.201206702
- Issue published online: 7 NOV 2012
- Article first published online: 16 OCT 2012
- Manuscript Received: 18 AUG 2012
- NIH. Grant Number: R01 GM67163
- Organic Syntheses
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