Abstract
A palladium-catalyzed tandem reaction of 7-oxabenzonorbornadienes with organic carboxylic acids that provides cis-1,2-dihydro-l-naphthyl derivatives in moderate to good yields in a highly diastereoselective manner is described. A possible reaction mechanism involving syn acylation followed by insertion and diastereoselective ring-opening with 7-oxabenzonorbornadienes is proposed to account for the reaction.
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