Issue 20, 2000

Palladium-catalyzed regioselective arylation of silyloxy compounds with triarylantimony diacetates

Abstract

The palladium-catalyzed arylation of enol silyl ethers, siloxydienes, silyloxycyclopropane with triarylantimony diacetates was carried out in the presence of PdCl2(CH3CN)2 (5 mol%) in DME–CH3CN at room temperature under mild conditions.

Article information

Article type
Communication
Submitted
07 Aug 2000
Accepted
15 Sep 2000
First published
28 Sep 2000

J. Chem. Soc., Perkin Trans. 1, 2000, 3350-3351

Palladium-catalyzed regioselective arylation of silyloxy compounds with triarylantimony diacetates

S. Kang, H. Ryu and Y. Hong, J. Chem. Soc., Perkin Trans. 1, 2000, 3350 DOI: 10.1039/B006431I

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