Support for this work was provided by the National Institute of General Medical Sciences (GM-72566). We are grateful to Li Li for obtaining mass spectrometric data for all compounds (MIT Department of Chemistry Instrumentation Facility, which is supported in part by the NSF (CHE-9809061 and DBI-9729592) and the NIH (1S10RR13886-01)).
Macrocyclization by Nickel-Catalyzed, Ester-Promoted, Epoxide–Alkyne Reductive Coupling: Total Synthesis of (−)-Gloeosporone†
Article first published online: 17 JUN 2009
Copyright © 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Volume 121, Issue 29, pages 5470–5472, July 6, 2009
How to Cite
Trenkle, James D. and Jamison, Timothy F. (2009), Macrocyclization by Nickel-Catalyzed, Ester-Promoted, Epoxide–Alkyne Reductive Coupling: Total Synthesis of (−)-Gloeosporone. Angew. Chem., 121: 5470–5472. doi: 10.1002/ange.200902079
- Issue published online: 1 JUL 2009
- Article first published online: 17 JUN 2009
- Manuscript Received: 17 APR 2009
- National Institute of General Medical Sciences. Grant Number: GM-72566
- NSF. Grant Numbers: CHE-9809061, DBI-9729592
- NIH. Grant Number: 1S10RR13886-01
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