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质量水平
方案
95%
旋光性
[α]22/D -50°, c = 1 in chloroform
折射率
n20/D 1.5513
密度
1.0459 g/mL at 25 °C
官能团
phenyl
储存温度
2-8°C
SMILES字符串
C[Si](C)(C)OC([C@@H]1CCCN1)(c2ccccc2)c3ccccc3
InChI
1S/C20H27NOSi/c1-23(2,3)22-20(19-15-10-16-21-19,17-11-6-4-7-12-17)18-13-8-5-9-14-18/h4-9,11-14,19,21H,10,15-16H2,1-3H3/t19-/m0/s1
InChI key
RSUHWMSTWSSNOW-IBGZPJMESA-N
应用
三组分反应和 α,β-不饱和醛的 Robinson 环化反应的有机催化剂。
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
The Journal of organic chemistry, 72(22), 8459-8471 (2007-10-09)
The highly enantioselective organocatalytic Robinson annulation of alpha,beta-unsaturated aldehydes was achieved, catalyzed by l-proline and trialkylamines and providing the formal [4 + 2] cycloaddition adducts. Additionally, in some examples in the catalysis with diarylpyrrolinol silyl ethers, the reactions afforded the
Chemical and Engineering News, June (2006)
Nature, 441(7095), 861-863 (2006-06-17)
Efficient and elegant syntheses of complex organic molecules with multiple stereogenic centres continue to be important in both academic and industrial laboratories. In particular, catalytic asymmetric multi-component 'domino' reactions, used during total syntheses of natural products and synthetic building blocks
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