登录 查看组织和合同定价。
选择尺寸
关于此项目
经验公式(希尔记法):
C33H30N2O2
化学文摘社编号:
分子量:
486.60
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352005
MDL number:
Assay:
95%
Form:
solid
InChI
1S/C33H30N2O2/c1-33(2,31-34-27(23-15-7-3-8-16-23)29(36-31)25-19-11-5-12-20-25)32-35-28(24-17-9-4-10-18-24)30(37-32)26-21-13-6-14-22-26/h3-22,27-30H,1-2H3/t27-,28-,29+,30+/m1/s1
SMILES string
CC(C1=N[C@H](C2=CC=CC=C2)[C@H](C3=CC=CC=C3)O1)(C)C4=N[C@H](C5=CC=CC=C5)[C@H](C6=CC=CC=C6)O4
InChI key
ZWWGNCSTEMMQOQ-XAZDILKDSA-N
assay
95%
form
solid
mp
164-169 °C
functional group
ether, phenyl
Quality Level
Application
(4R,4′R,5S,5′S)-2,2′-(1-Methylethylidene) or (4S,5R)-Bis-Phbox) can be used as a ligand:
This chiral Box ligand was most recently shown to mediate an asymmetric aminofluorination of olefins utlizing Xtalfuor-E (719439) and TREAT-HF (344648). The resulting cyclic carbamates can be readily converted into their concomitant beta-fluoro amino acids.
- To prepare selective exo-catalysts for enantioselective 1,3-dipolar cycloaddition reactions.
- In the asymmetric aminooxygenation of alkenes in the presence of tetramethylaminopyridyl radical (TEMPO) as an oxidant and copper(II) triflate as a catalyst.
- In asymmetric aminofluorination of olefins using an iron catalyst.
This chiral Box ligand was most recently shown to mediate an asymmetric aminofluorination of olefins utlizing Xtalfuor-E (719439) and TREAT-HF (344648). The resulting cyclic carbamates can be readily converted into their concomitant beta-fluoro amino acids.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Iron (II)-catalyzed intramolecular olefin aminofluorination
Lu Deng-Fu, et al.
Organic Letters, 16(11), 2912-2915 (2014)
Copper catalyzed enantioselective intramolecular aminooxygenation of alkenes
Fuller PH, et al.
Journal of the American Chemical Society, 130(52), 17638-17639 (2008)
In Search of exo-Selective Catalysts for Enantioselective 1, 3-Dipolar Cycloaddition between Acryloyloxazolidinone and Diphenylnitrone
Desimoni G, et al.
European Journal of Organic Chemistry, 2005(6), 1020-1027 (2005)
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持