烷基化
化学
催化作用
组合化学
卤化物
范围(计算机科学)
甲基化
三唑
小学(天文学)
有机化学
计算机科学
程序设计语言
天文
生物化学
基因
物理
作者
Gianpiero Cera,Tobias Haven,Lutz Ackermann
标识
DOI:10.1002/ange.201509603
摘要
Abstract Triazole assistance set the stage for a unified strategy for the iron‐catalyzed C−H allylation of arenes, heteroarenes, and alkenes with ample scope. The versatile catalyst also proved competent for site‐selective methylation, benzylation, and alkylation with challenging primary and secondary halides. Triazole‐assisted C−H activation proceeded chemo‐, site‐, and diastereo‐selectively, and the modular TAM directing group was readily removed in a traceless fashion under exceedingly mild reaction conditions.
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