![((4S,5S)-(-)-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% (S,S)-[COD]Ir[c,((4S,5S)-(-)-O-[1-苄基-1-(5-甲基-2-苯基-4,5-二氢恶唑-4-基)-2-苯基乙基]-二环己基磷)(1,5-COD)铱 (I) 四三(3,5-双(三氟甲基)苯硼酸 , min. 97%](https://static.jkchemical.com/Structure/100/100448.png)
((4S,5S)-(-)-O-[1-苄基-1-(5-甲基-2-苯基-4,5-二氢恶唑-4-基)-2-苯基乙基]-二环己基磷)(1,5-COD)铱 (I) 四三(3,5-双(三氟甲基)苯硼酸 , min. 97%
((4S,5S)-(-)-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% (S,S)-[COD]Ir[c
分子式: Ir(C8H12)(C37H46NO2P)+B[C6H3(CF3)2]4ae
分子量: 1731.35
纯度: min. 97%
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基本信息
安全信息
化学和物理性质
产品描述
Technical Notes:
1. Iridium-catalyzed asymmetric hydrogenation of N-protected indoles.
2.Iridium-catalyzed asymmetric hydrogenation of unfunctionalized enamines .
3.L igand for Ir-catalyzed Asymmetric Hydrogenation of 1-Silyl-1-substituted Alkenes .
References:
1.Chem-Eur. J., 2010, 16, 2036.
2.Chem-Eur. J.. 2009, 15, 2266.
3.Tetrahedron L ett. 2016, 57, 5666- 5668.
