化学
废止
催化作用
齿合度
配体(生物化学)
位阻效应
过渡金属
药物化学
组合化学
氧气
立体化学
金属
有机化学
受体
生物化学
作者
Hyun Tae Kim,Eunsu Kang,Minkyu Kim,Jung Min Joo
出处
期刊:Organic Letters
[American Chemical Society]
日期:2021-04-12
卷期号:23 (9): 3657-3662
被引量:34
标识
DOI:10.1021/acs.orglett.1c01040
摘要
A new class of bidentate ligands was prepared by a modular approach involving Rh-catalyzed C-H annulation reactions. The resulting conformationally constrained ligands enabled the Pd-catalyzed C-H alkenylation at electron-rich and sterically less hindered positions of electron-rich arenes while promoting the facile oxidation of Pd(0) intermediates by oxygen. This newly introduced ligand class is complementary to the ligands developed for Pd-catalyzed oxidative reactions and may find broad application in transition-metal-catalyzed reactions.
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