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Benzannulation from alkynes and allyl tosylates via a pi-allylpalladium intermediate
Authors:Tsukada  Sugawara  Inoue
Institution:Department of Materials Chemistry, Graduate School of Engineering, Tohoku University, Sendai, Japan. tsukada@aporg.che.tohoku.ac.jp
Abstract:reaction: see text] Allyl tosylate is a good allyl source for a novel palladium-catalyzed benzannulation that affords polysubstituted benzenes from 1 mol of an allyl compound and 2 mol of internal alkynes. Using triphenyl phosphite as a ligand, the reaction with terminal alkynes gave trisubstituted benzenes regioselectively.
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