![((4R,5R)-(+)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydrooxazol-4-yl)-2-phenylethyl] (dicyclohexylphosphinite)(1,5-COD)iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenylborate, min. 97% (R,R)-[COD]Ir[,((4R,5R)-(+)-O-[1-苯甲基-1-(5-甲基-2-苯基-4,5-二氢恶唑-4-基)-2-苯基乙基](二环己基膦亚盐)(1,5-COD)铱(I)四(3,5-二(三氟甲基)苯基硼酸 , min. 97%](https://static.jkchemical.com/Structure/792/792710.png)
((4R,5R)-(+)-O-[1-苯甲基-1-(5-甲基-2-苯基-4,5-二氢恶唑-4-基)-2-苯基乙基](二环己基膦亚盐)(1,5-COD)铱(I)四(3,5-二(三氟甲基)苯基硼酸 , min. 97%
((4R,5R)-(+)-O-[1-Benzyl-1-(5-methyl-2-phenyl-4,5-dihydrooxazol-4-yl)-2-phenylethyl] (dicyclohexylphosphinite)(1,5-COD)iridium(I) tetrakis(3,5-bis(trifluoromethyl)phenylborate, min. 97% (R,R)-[COD]Ir[
分子式: Ir(C₈H₁₂)(C₃₇H₄₆NO₂P)⁺B[C₆H₃(CF₃)₂]
分子量: 1731.35
纯度: min. 97%
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基本信息
安全信息
存储条件Store at 2-8℃ |
化学和物理性质
产品描述
Technical Note:
1. New class of hydrogenation catalyst which can convert unfunctionalized styrenyl olefins into alkanes with excellent enantioselectivity.
2. Ligand for Ir-catalyzed Asymmetric Hydrogenation of 1-Silyl-1 -substituted Alkenes.
References:
1. Adv. Synth. Catal., 2002, 344, 40.
2. Acc. Chem. Res., 2007, 40, 1402.
3. Tetrahedron L ett. 2016, 57, 5666 5668.
