Journal
CHEMICAL COMMUNICATIONS
Volume 49, Issue 52, Pages 5892-5894Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc42823k
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Funding
- National Natural Science Foundation of China [21125206, 21021001]
- Third Military Medical University [2012XZH06]
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An aminocatalytic asymmetric Diels-Alder reaction of 2,4-dienals and labile 1-indenones in situ generated from 3-bromo-1-indanones was developed, producing highly fused indane products with multiple chiral centres followed by a cascade N-heterocyclic carbene-mediated benzoin condensation.
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