期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 131, 期 30, 页码 10386-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja904365h
关键词
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资金
- European Commission [MEST-C7-2005-020744]
The versatility of chiral copper hydride catalysis has been demonstrated through development of highly enantioselective 1,4-reductions of 2-alkenytheteroarenes, substrates that have been rarely considered for asymmetric conjugate addition reactions. Both azoles and azines serve as efficient activating groups for this process.
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