Pd-Catalyzed Ring Opening of Oxa- and Azabicyclic Alkenes with Aryl and Vinyl Halides: Efficient Entry to 2-Substituted 1,2-Dihydro-1-naphthols and 2-Substituted 1-Naphthols
作者:Chi-Li Chen、Stephen F. Martin
DOI:10.1021/jo060299p
日期:2006.6.1
1,2-dihydronaphthols in good to excellent yields. These reactions occurred under very mild conditions with a variety of arylhalides bearing electron-withdrawing or -donating groups. Similarly, a 7-azabenzonorbornadiene substituted with an electron-withdrawing group on the nitrogen atom underwent facile ring-opening reaction with arylhalides to provide cis-2-substitued (1,2-dihydro-1-naphthyl)carbamates