Y. Tada, Akiharu Satake, I. Shimizu*
Dec 1, 1996
Citations
0
Influential Citations
18
Citations
Journal
Chemistry Letters
Abstract
C-Allylation of 1- or 2-naphthols to give mono-, di-, and triallylnaphthols selectively using allylic alcohols directly under neutral conditions has been realized by employing palladium catalysts in the presence of molecular sieve 4A. This method is also applicable for the multiple allylation of 2,6-dihydroxynaphthalene.