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Palladium-catalyzed annulation of arynes by 2-halobenzaldehydes: synthesis of fluoren-9-ones.

Organic letters (2005-08-27)
Xiaoxia Zhang, Richard C Larock
RESUMEN

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. [reaction: see text]

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Sigma-Aldrich
9-Fluorenone, 98%
Sigma-Aldrich
2-Bromobenzaldehyde, 98%