Organic Ligand-Free Alkylation of Amines, Carboxamides, Sulfonamides, and Ketones by Using Alcohols Catalyzed by Heterogeneous Ag/Mo Oxides

被引:176
作者
Cui, Xinjiang [1 ,2 ]
Zhang, Yan [1 ]
Shi, Feng [1 ]
Deng, Youquan [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, Ctr Green Chem & Catalysis, Lanzhou 730000, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100049, Peoples R China
关键词
Ag/Mo; amines; carboxamides; ketones; sulfonamides; N-ALKYLATION; ARYL HALIDES; BORROWING HYDROGEN; DIRECT AMINATION; AMIDE SYNTHESIS; INTRAMOLECULAR HYDROAMINATION; RUTHENIUM COMPLEXES; DIRECT SUBSTITUTION; ALLYLIC ALCOHOLS; AROMATIC-AMINES;
D O I
10.1002/chem.201001915
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Complicated and expensive organic ligands are normally essential in fine chemical synthesis at preparative or industrial levels. The synthesis of fine chemicals by using heterogeneous catalyst systems without additive organic ligand is highly desirable but severely limited due to their poor generality and rigorous reaction conditions. Here, we show the results of carbon nitrogen or carbon carbon bond formation catalyzed by an Ag/Mo hybrid material with specific Ag6Mo10O33 crystal structure. 48 nitrogen- or oxygen-containing compounds, that is, amines, carboxamides, sulfonamides, and ketones, were successfully synthesized through a borrowing-hydrogen mechanism. Up to 99% isolated yields were obtained under relatively mild conditions without additive organic ligand. The catalytic process shows promise for the efficient and economic synthesis of amine, carboxamide, sulfonamide, and ketone derivatives because of the simplicity of the system and ease of operation.
引用
收藏
页码:1021 / 1028
页数:8
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