Journal
ORGANIC LETTERS
Volume 15, Issue 9, Pages 2250-2253Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol400821q
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Funding
- 973 Program [2011CB808600]
- National Natural Science Foundation of China [20972117, 21172176]
- Fundamental Research Funds for the Central Universities
- Large-scale Instrument And Equipment Sharing Foundation of Wuhan University
- [NCET-10-0649]
- [IRT1030]
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An unprecedented Ag(I)-catalyzed asymmetric desymmetrization of Spiro cyclohexadienone lactones has been developed successfully, which performs well over a broad scope of substrates and provides a facile access to optically active spirolactone-pyrrolidines in high yields with excellent levels of diastereo-/enantioselectivities.
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