Bioactive 2‐benzazepines were accessed in an atom‐ and step‐economical manner through a versatile palladium‐catalyzed C−H activation strategy. The C−H arylation required low catalyst loading and a mild base, which was reflected by a broad scope and high functional‐group tolerance. The benzotriazolodiazepinones were identified as new heat shock protein 90 (Hsp90) inhibiting lead compounds, with considerable
生物活性的2-苯并ze庚因是通过通用的
钯催化的CH活化方法以原子经济和分步经济的方式获得的。CH芳基化反应需要低的催化剂负载量和适度的碱,这反映在宽范围和高官能团耐受性上。苯并三唑并二氮杂
吡啶酮被鉴定为新的抑制热激蛋白90(Hsp90)的先导化合物,在抗癌应用中具有相当大的潜力。