化学
硼酸化
区域选择性
蒽醌类
铱
催化作用
蒽醌
磺胺
选择性
组合化学
药物化学
有机化学
植物
生物
烷基
芳基
作者
Andrew M. Camelio,Robert Wright,Nicole T. Knight,B.A. Jazdzewski
标识
DOI:10.1021/acs.joc.9b00106
摘要
A mild, regioselective, iridium-catalyzed C-H amidation and borylation of anthraquinones to the o-sulfonamide and m-borylated products has been developed. The anthraquinone carbonyl moieties direct the C-H amidation with high selectivity to afford the ortho-substituted products in modest to high yields.
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