(4R,4′R,5S,5′S)-2,2′-(1-Methylethylidene

产品名称：

157904-67-1
(4R,4′R,5S,5′S)-2,2′-(1-Methylethylidene
2,2-Bis[2-(4R,5S-diphenyl-1,3-oxazolinyl)]propane

产品介绍：

产品说明

应用

(4R,4′R,5S,5′S)-2,2′-(1-Methylethylidene) or (4S,5R)-Bis-Phbox) can be used as a ligand:

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.

包装

250 mg in amber glass bottle

其他说明

Iron(II)-Catalyzed Intramolecular Olefin Aminofluorination

基本信息

经验(实验)分子式	C₃₃H₃₀N₂O₂
分子量	486.60
MDL编号	MFCD24849939
PubChem化学物质编号	329768502
NACRES	NA.22

产品性质

质量水平	100
测定	95%
mp	164-169 ℃
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	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
InChI key	ZWWGNCSTEMMQOQ-XAZDILKDSA-N

安全信息

储存分类代码	13 - Non Combustible Solids
WGK	WGK 3
闪点(F)	Not applicable
闪点(C)	Not applicable