Journal
ORGANIC LETTERS
Volume 7, Issue 18, Pages 3973-3976Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ol0514597
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- NIGMS NIH HHS [GM 070620] Funding Source: Medline
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Arynes, generated in situ from 2-(trimethylsilyl)aryl triflates and CsF, undergo annulation by o-haloarenecarboxaldehydes in the presence of a Pd catalyst, providing a useful new method for the synthesis of fluoren-9-ones in good yields.
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