Journal
CHEMICAL SCIENCE
Volume 4, Issue 12, Pages 4499-4504Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3sc52379a
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Funding
- MEXT, Japan
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Enantioselective [3 + 2] annulation between 1,3-dienes and N-acyl ketimines in situ generated from 3-aryl-3-hydroxyisoindolin-1-ones proceeded via C-H activation to give spiroaminoindane derivatives in high yields with high regio-and enantioselectivity, which is realized by use of an Ir/chiral diene catalyst.
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