废止
对映体药物
降冰片烯
芳基
化学
催化作用
钯
环氧化物
组合化学
有机化学
对映选择合成
共聚物
聚合物
烷基
作者
Renhe Li,Guangbin Dong
标识
DOI:10.1002/anie.201712393
摘要
Abstract Herein we report a direct annulation between aryl iodides and epoxides through palladium/norbornene (Pd/NBE) cooperative catalysis. An iso‐propyl ester substituted NBE was found to be most efficient to suppress the formation of multiple‐NBE‐insertion byproducts and affords the desired 2,3‐dihydrobenzofuran derivatives in 44–99 % yields. The reaction is scalable and tolerates a range of functional groups. Asymmetric synthesis is realized using an enantiopure epoxide. Application of this method into a concise synthesis of insecticide fufenozide is demonstrated.
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