反式,反式-1,5-双[4-(三氟甲基)苯基]-1,4-戊二烯-3-酮
![反式,反式-1,5-双[4-(三氟甲基)苯基]-1,4-戊二烯-3-酮结构式](https://image.chemsrc.com/caspic/440/103836-71-1.png)
反式,反式-1,5-双[4-(三氟甲基)苯基]-1,4-戊二烯-3-酮结构式
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常用名 | 反式,反式-1,5-双[4-(三氟甲基)苯基]-1,4-戊二烯-3-酮 | 英文名 | trans,trans-1,5-Bis[4-(trifluoromethyl)phenyl]-1,4-pentadien-3-one |
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| CAS号 | 103836-71-1 | 分子量 | 370.28800 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C19H12F6O | 熔点 | N/A | |
| MSDS | 中文版 美版 | 闪点 | N/A | |
| 符号 |
GHS06 |
信号词 | Danger |
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Highly Enantioselective Synthesis of Spiro[cyclohexanone-oxindoles] and Spiro[cyclohexanone-pyrazolones] by Asymmetric Cascade [5+1] Double Michael Reactions Bin Wu, Jian Chen, Mei-Qiu Li, Jin-Xin Zhang, et al.
European J. Org. Chem. 7 , 1318-1327, (2012)
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Asymmetric organocatalytic double-conjugate addition of malononitrile to dienones: efficient synthesis of optically active cyclohexanones.
Org. Lett. 13(3) , 374-377, (2011) 9-Amino-9-deoxyepiquinine efficiently catalyzed the double-conjugate addition of malononitrile to dienones. A number of 1,1,2,6-tetrasubstituted cyclohexanones were prepared in good yields, diastereoselectivities, and excellent enantioselectivities. |
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Synthesis of optically enriched spirocyclic benzofuran-2-ones by bifunctional thiourea-base catalyzed double-Michael addition of benzofuran-2-ones to dienones.
Chem. Asian J. 8(5) , 997-1003, (2013) A highly enantioselective catalytic double-Michael addition reaction of substituted benzofuran-2-ones with divinyl ketones promoted by readily accessible tertiary amine-thiourea Cinchona alkaloids has been developed. A number of optically enriched spirocyclic... |