Journal
CHEMICAL COMMUNICATIONS
Volume 48, Issue 88, Pages 10913-10915Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c2cc36048a
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Funding
- National Natural Science Foundation of China [21172206, 20972147]
- National Basic Research Program of China (973 Program) [2010CB833300]
- Program for Changjiang Scholars and Innovative Research Team in University [IRT1189]
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A range of arylallenes undergo carbocation-initiated cyclization reaction with N-benzylic and N-allylic sulfonamides in the presence of 10 mol% ferric chloride to give structurally diverse polysubstituted indenes in good yields with extremely high regioselectivity.
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