Journal
ORGANIC LETTERS
Volume 10, Issue 9, Pages 1767-1770Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol800450x
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Novel Hg(OTf)(2)-Catalyzed arylene cyclization was achieved with highly efficient catalytic turnover (up to 200 times). The reaction takes place via protonation of allylic hydroxyl group by in situ formed TfOH of an organomercuric intermediate to generate a cationic species. Subsequent smooth demercuration regenerates the catalyst.
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