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• W2900599883 abstract "Conditions allowing the C10- and C11-arylations of dibenzo[b,f]azepines via successive palladium-catalyzed reactions are reported. Using aryl bromides as the aryl source, the C10-arylation of dibenzo[b,f]azepines is very selective. Then, using benzenesulfonyl chlorides as the aryl source, the second arylation at C11-position is achieved affording non-symmetrical C10,C11-diarylated dibenzo[b,f]azepines. Both reactions tolerate a variety of substituents on the aryl source." @default.
• W2900599883 created "2018-11-29" @default.
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• W2900599883 date "2018-12-28" @default.
• W2900599883 modified "2023-09-27" @default.
• W2900599883 title "Convenient Access to C10- and C11-(di)arylated dibenzo[<i>b</i> ,<i>f</i> ]azepines <i>via</i> Palladium-catalyzed C−H Bonds Cleavages" @default.
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• W2900599883 doi "https://doi.org/10.1002/adsc.201801366" @default.
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