Gold(I)-Catalyzed Intramolecular Hydroamination of Alkenyl Carbamates
Xiaoqing Han, Ross A. Widenhoefer*
*P. M. Gross Chemical Laboratory, Duke University, Durham, NC 27708-0346, USA, Email: rwidenhochem.duke.edu
X. Han, R. A. Widenhoefer, Angew. Chem. Int. Ed., 2006, 45, 1747-1749.
DOI: 10.1002/anie.200600052
Abstract
A mild, effective gold(I)-catalyzed hydroamination of unactivated olefins to form protected nitrogen heterocycles has been developed. The substrate scope is broader than in reactions realized with late-transition-metal catalyst systems.
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C. F. Bender, R. A. Widenhoefer, Org. Lett., 2006, 8, 5303-5305.
Z. Zhang, C. Liu, R. E. Kinder, X. Han, H. Qian, R. A. Widenhoefer, J. Am. Chem. Soc., 2006, 128, 9066-9073.
Key Words
alkenes, amines, gold, homogeneous catalysis, hydroamination, cyclic amines
ID: J06-Y2006-660