期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 131, 期 37, 页码 13226-13227出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja905213f
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资金
- National Science Foundation [CHE-0911192]
- Rutgers, The State University of New Jersey
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [0911192] Funding Source: National Science Foundation
The first example of a catalytic enantioselective intramolecular hydride shift/ring closure reaction is reported. This redox neutral reaction cascade allows for the efficient formation of ring-fused tetrahydroquinolines in high enantioselectivities.
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