Manganese-Catalyzed Transfer Hydrodebromination of Aryl Bromides with Ethanol

被引:2
作者
Wen, Xiaoting [1 ]
Gong, Yingjie [1 ]
Niu, Shuodong [1 ]
Luo, Tianjun [1 ]
Xi, Hui [2 ]
Liu, Weiping [1 ]
机构
[1] Donghua Univ, Coll Chem & Chem Engn, Minist Educ, Key Lab Sci & Technol Ecotext, Shanghai 201620, Peoples R China
[2] Zhengzhou Tobacco Res Inst CNTC, Key Lab Tobacco Flavor Basic Res CNTC, Zhengzhou 450001, Peoples R China
基金
中国国家自然科学基金; 上海市自然科学基金;
关键词
debromination; ethanol; homogeneous catalysis; manganese; transfer hydrogenation; SUSTAINABLE SYNTHESIS; BORROWING HYDROGEN; DEHALOGENATION; PINCER; HYDRODEHALOGENATION; ALKYL; REDUCTION; HALIDES; COMPLEXES; ALCOHOLS;
D O I
10.1002/ejoc.202201376
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A convenient PNP pincer manganese catalyzed transfer hydrogenation of bromides to corresponding debrominated aryl compounds using ethanol as the hydrogen sources is reported. Importantly, the application of biomass-derived ethanol highlights the sustainability of the methodology. The use of 6-phenyl substituted triazine-based (PNPipr)-N-ipr-P-5 manganese pincer catalyst allows for the debromination of various aryl bromides with good yields. Notably, the process also occurs with bromides derived from several classes of natural products and bioactive compounds, such as citronellol, diacetone fructose, cholesterol, and vitamin E.
引用
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页数:5
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