烯醇
卤化物
催化作用
化学
镍
化学计量学
卤化
吡啶
药物化学
有机化学
作者
Julie L. Hofstra,Kelsey E. Poremba,Alex M. Shimozono,Sarah E. Reisman
标识
DOI:10.1002/anie.201906815
摘要
Abstract A Ni‐catalyzed halogenation of enol triflates was developed and it enables the synthesis of a broad range of alkenyl iodides, bromides, and chlorides under mild reaction conditions. The reaction utilizes inexpensive, bench‐stable Ni(OAc) 2 ⋅4 H 2 O as a precatalyst and proceeds at room temperature in the presence of sub‐stoichiometric Zn and either 1,5‐cyclooctadiene or 4‐( N , N ‐dimethylamino)pyridine.
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