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School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo 192-0392, Japan
E-mail: yanai@toyaku.ac.jp
; Fax: +81 676 3257
; Tel: +81 676 3257
Chem. Commun., 2012,48, 8967-8969
DOI:
10.1039/C2CC33606E
Received
18 May 2012,
Accepted
18 Jul 2012
First published online
18 Jul 2012
(Z)-Selective olefination of several lactones with ketene silyl acetals was achieved by the catalysis of carbon acids (C–H acids) having a bis(triflyl)methyl group as an acidic functionality; in particular, the triple carbon acid having three bis(triflyl)methyl groups in phloroglucinol shows an excellent catalytic performance.