化学
废止
区域选择性
催化作用
钴
配体(生物化学)
终端(电信)
组合化学
立体化学
药物化学
有机化学
受体
生物化学
计算机科学
电信
作者
Gang Qian,Ran Chen,Tingting Miao,Yonghong Xiao,Sanliang Li,Wenhua Gao,Jian‐Ji Zhong
标识
DOI:10.1021/acs.orglett.5c02125
摘要
The annulation of o-haloaromatic ketones with terminal alkynes to access indenols remains a persistent challenge, with limited successful precedents reported to date. Herein, we disclose a cobalt-catalyzed ligand-controlled strategy for the divergent synthesis of indenols. By simple modulation of the ligand, the annulation of o-iodoaromatic ketones with terminal alkynes can be selectively achieved toward either 2- or 3-substituted indenols. This approach features excellent regioselectivity, a broad substrate scope, and late-stage modification.
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