Ruthenium-Catalyzed Gram-Scale Preferential C-H Arylation of Tertiary Phosphine

被引:36
作者
Li, Jia-Wei [1 ,2 ]
Wang, Liang-Neng [1 ,2 ]
Li, Ming [1 ,2 ]
Tang, Pan-Ting [1 ,2 ]
Luo, Xiao-Peng [1 ,2 ]
Kurmoo, Mohamedally [4 ]
Liu, Yue-Jin [1 ,2 ]
Zeng, Ming-Hua [1 ,2 ,3 ]
机构
[1] Hubei Univ, Hubei Collaborat Innovat Ctr Adv Chem Mat, Key Lab Synth & Applicat Organ Funct Mol, Minist Educ, Wuhan 430062, Hubei, Peoples R China
[2] Hubei Univ, Coll Chem & Chem Engn, Wuhan 430062, Hubei, Peoples R China
[3] Guangxi Normal Univ, Dept Key Lab Chem & Mol Engn Med Resources, Sch Chem & Pharmaceut Sci, Guilin 541004, Peoples R China
[4] Univ Strasbourg, CNRS, Inst Chim Strasbourg, UMR7177, 4 Rue Blaise Pascal, F-67070 Strasbourg, France
基金
美国国家科学基金会;
关键词
D O I
10.1021/acs.orglett.9b00888
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A general protocol for site-preferential mono-C-H arylation of tertiary phosphine ligands catalyzed by a ruthenium(II) complex was devised. This protocol gives access to a series of modified Buchwald-biaryl monophosphines on a gram scale in moderate to excellent yields. A catalytic cycle is proposed derived from knowledge of the intermediates observed by ESI-MS. Importantly, these monoarylated products could be further transformed into dibenzophosphole derivatives.
引用
收藏
页码:2885 / 2889
页数:5
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