N-[3,5-二(三氟甲基)苯基]-N'-[(9R)-6'-甲氧基奎宁-9-基]硫脲
![N-[3,5-二(三氟甲基)苯基]-N'-[(9R)-6'-甲氧基奎宁-9-基]硫脲结构式](https://image.chemsrc.com/caspic/373/852913-25-8.png)
N-[3,5-二(三氟甲基)苯基]-N'-[(9R)-6'-甲氧基奎宁-9-基]硫脲结构式
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常用名 | N-[3,5-二(三氟甲基)苯基]-N'-[(9R)-6'-甲氧基奎宁-9-基]硫脲 | 英文名 | 1-(3,5-BIS(TRIFLUOROMETHYL)PHENYL)-3-((1R)-(6-METHOXYQUINOLIN-4-YL)((2R,4S,5R)-5-VINYLQUINUCLIDIN-2-YL)METHYL)THIOUREA |
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| CAS号 | 852913-25-8 | 分子量 | 594.61400 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C29H28F6N4OS | 熔点 | 150°C | |
| MSDS | 中文版 美版 | 闪点 | N/A | |
| 符号 |
GHS06 |
信号词 | Danger |
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Urea- and thiourea-substituted cinchona alkaloid derivatives as highly efficient bifunctional organocatalysts for the asymmetric addition of malonate to nitroalkenes: inversion of configuration at C9 dramatically improves catalyst performance.
Angew. Chem. Int. Ed. Engl. 44 , 6367-6370, (2005)
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Highly enantioselective conjugate addition of nitromethane to chalcones using bifunctional cinchona organocatalysts.
Org. Lett. 7 , 1967-1969, (2005) Cinchona alkaloid-derived chiral bifunctional thiourea organocatalysts were synthesized and applied in the Michael addition between nitromethane and chalcones with high ee and chemical yields. |
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