化学
区域选择性
酮
催化作用
分子间力
电泳剂
共轭体系
组合化学
钴
立体化学
分子
有机化学
聚合物
作者
Md Raja Sk,Sourav Sekhar Bera,Modhu Sudan Maji
出处
期刊:Organic Letters
[American Chemical Society]
日期:2017-12-19
卷期号:20 (1): 134-137
被引量:73
标识
DOI:10.1021/acs.orglett.7b03440
摘要
Weakly coordinating, ketone-directed, regioselective monoallylation of arenes and indoles is reported using a stable and cost-effective high-valent cobalt(III)-catalyst to access several important molecular building blocks. The allylation proceeds smoothly with a variety of substrates in the presence of various electron-rich and -deficient substituents. The method was applied to the formal synthesis of an ancisheynine alkaloid, a highly conjugated azatetracene, and isochroman. The mechanistic study reveals that the allylation reaction follows a base-assisted intermolecular electrophilic substitution pathway.
科研通智能强力驱动
Strongly Powered by AbleSci AI