中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
—— | (m-nitrobenzylidene)-p-bromoaniline | 3489-08-5 | C13H9BrN2O2 | 305.131 |
3-硝基苯甲醇 | 3-Nitrobenzyl alcohol | 619-25-0 | C7H7NO3 | 153.137 |
N-苄叉苯胺 | N-benzylideneaniline | 538-51-2 | C13H11N | 181.237 |
间硝基苯甲醛 | 3-nitro-benzaldehyde | 99-61-6 | C7H5NO3 | 151.122 |
中文名称 | 英文名称 | CAS号 | 化学式 | 分子量 |
---|---|---|---|---|
1-(3-硝基苯基)-N-(4-硝基苯基)甲亚胺 | (3-nitro-benzylidene)-(4-nitro-phenyl)-amine | 17064-97-0 | C13H9N3O4 | 271.232 |
—— | (m-nitrobenzylidene)-p-bromoaniline | 3489-08-5 | C13H9BrN2O2 | 305.131 |
—— | (3-Nitrobenzyl)(3-nitrobenzylidene)amine | 10480-08-7 | C13H9N3O4 | 271.232 |
—— | 3-nitrobenzaldoxime | 3717-30-4 | C7H6N2O3 | 166.136 |
—— | 3-Nitro-benzalazin | 40252-71-9 | C14H11N3O2 | 253.26 |
—— | (E)-1-(4-bromophenyl)-2-(3-nitrobenzylidene)hydrazine | 105946-52-9 | C13H10BrN3O2 | 320.145 |
N-苄叉苯胺 | N-benzylideneaniline | 538-51-2 | C13H11N | 181.237 |
间硝基苯甲醛 | 3-nitro-benzaldehyde | 99-61-6 | C7H5NO3 | 151.122 |
First osmium-catalyzed reductive amination under the water gas–shift reaction conditions was developed. Proposed catalytic system demonstrates high performance even at the catalyst loading as low as 0.0625 mol%.
In this research, nano magnetic sulfated zirconia was prepared through a green and facile method and acted as a novel, heterogeneous, efficient nano-catalyst for the one-pot three component synthesis of α-aminonitrile derivatives.