Kim Hyun Tae, Kang Eunsu, Kim Minkyu, Joo Jung Min
Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University, Busan 46241, Republic of Korea.
Org Lett. 2021 May 7;23(9):3657-3662. doi: 10.1021/acs.orglett.1c01040. Epub 2021 Apr 12.
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.
通过涉及铑催化的C-H环化反应的模块化方法制备了一类新型双齿配体。所得的构象受限配体能够在富电子芳烃的富电子且空间位阻较小的位置进行钯催化的C-H烯基化反应,同时促进钯(0)中间体被氧气的 facile 氧化。这种新引入的配体类别与为钯催化的氧化反应开发的配体互补,可能在过渡金属催化的反应中得到广泛应用。
“facile”在这里可能不太好准确翻译,暂保留英文,可根据具体语境进一步优化,比如“容易的”“ facile的氧化”可理解为“易于发生的氧化” 。