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Palladium-Catalyzed Benzylic Arylation of N-Benzylxanthone Imine

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journal contribution
posted on 16.10.2008, 00:00 by Takashi Niwa, Hideki Yorimitsu, Koichiro Oshima
The direct benzylic arylation of N-benzylxanthone imine with aryl chloride proceeds under palladium catalysis, yielding the corresponding coupling product. The product is readily transformed to benzhydrylamine. Taking into consideration that the imine is readily available from benzylic amine, the overall transformation represents a formal cross-coupling reaction of aryl halide with α-aminobenzyl metal.

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