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质量水平
方案
96%
表单
solid
mp
99-103 °C
官能团
carboxylic acid
fluoro
SMILES字符串
OC(=O)C(F)(F)F.CN1[C@H](NCC1=O)C(C)(C)C
InChI
1S/C8H16N2O.C2HF3O2/c1-8(2,3)7-9-5-6(11)10(7)4;3-2(4,5)1(6)7/h7,9H,5H2,1-4H3;(H,6,7)/t7-;/m0./s1
InChI key
HKHKOEMMPVPVOS-FJXQXJEOSA-N
一般描述
(S)-(+)-2-(tert-Butyl)-3-methyl-4-imidazolidinone trifluoroacetic acid is a Macmillan imidazolidinone organocatalyst, which is generally employed in asymmetric transformation reactions.
应用
1,3-偶极加成反应和 Friedel-Crafts 烷基化反应的高选择性有机催化剂。
法律信息
适用美国专利 6,369,243 和相关专利。仅供研究使用。
警示用语:
Warning
危险声明
危险分类
Acute Tox. 4 Oral - Eye Irrit. 2
储存分类代码
11 - Combustible Solids
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
Highly enantioselective transfer hydrogenation of alpha, beta-unsaturated ketones
Journal of the American Chemical Society, 128(41), 13368-13369 (2006)
Journal of the American Chemical Society, 122, 9874-9874 (2000)
Modern strategies in organic catalysis: the advent and development of iminium activation.
Aldrichimica Acta, 39(3), 79-87 (2006)
New strategies in organic catalysis: the first enantioselective organocatalytic Friedel-Crafts alkylation.
Journal of the American Chemical Society, 123(18), 4370-4371 (2001-07-18)
商品
Discover Professor David MacMillan's groundbreaking metal-free asymmetric catalysis using imidazolidinone-based organocatalysts for versatile transformations.
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