化学
区域选择性
咔唑
催化作用
嘧啶
基质(水族馆)
药物化学
芳基
有机化学
组合化学
立体化学
烷基
海洋学
地质学
作者
Sonbidya Banerjee,Pinaki Bhusan De,Sourav Pradhan,Tariq A. Shah,Tharmalingam Punniyamurthy
标识
DOI:10.1002/ejoc.201801829
摘要
Ru II ‐catalysed pyrimidine directed coupling of the C‐7 C–H bond of indolines with acyl azides as a nitrogen surrogate has been developed to produce acyl amides at room temperature. The reaction of aryl, heteroaryl and α,β‐unsaturated acyl azides can be accomplished in good yields. The procedure can be extended to the C1‐amidation of carbazole with moderate yields. The substrate scope, use of less expensive Ru‐catalysis, and oxidant‐free conditions are the significant practical features.
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