(R,R,S)-DIAZAPHOS-PPE 2,2′-[(1R,3R)-2,3,5,10-四氢-5,10-二氧-2-苯基-1H-[1,2,4]二氮杂磷杂环戊烷[1,2-b]酞嗪-1,3-二基]双[N-[(1S)-1-苯乙基]苯甲酰胺]
CAS 615257-74-4 MFCD10566993
化学结构图
SMILES: C[C@H](NC(=O)C1=CC=CC=C1[C@@H]1N2C(=O)C3C=CC=CC=3C(=O)N2[C@@H](C2=CC=CC=C2C(=O)N[C@@H](C)C2C=CC=CC=2)P1C1C=CC=CC=1)C1C=CC=CC=1
化学属性
| Mol. Formula | C46H39N4O4P |
|---|---|
| Mol. Weight | 742.80 |
| Melting Point | 258-262 °C |
别名和识别编码
| Chemical Name | (R,R,S)-DiazaPhos-PPE |
|---|---|
| Synonym | (R,R,S)-DiazaPhos-PPE 2,2′-[(1R,3R)-2,3,5,10-四氢-5,10-二氧-2-苯基-1H-[1,2,4]二氮杂磷杂环戊烷[1,2-b]酞嗪-1,3-二基]双[N-[(1S)-1-苯乙基]苯甲酰胺] |
| MDL Number | MFCD10566993 |
| CAS Number | 615257-74-4 |
| Chemical Name Translation | 2,2′-[(1R,3R)-2,3,5,10-四氢-5,10-二氧-2-苯基-1H-[1,2,4]二氮杂磷杂环戊烷[1,2-b]酞嗪-1,3-二基]双[N-[(1S)-1-苯乙基]苯甲酰胺] |
| PubChem Substance ID | 329760941 |
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分类
- {SNA} Asymmetric Synthesis, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, Hydroformylation, Landis Ligands, Privileged Ligands and Complexes
- Asymmetric Synthesis, Chemical Synthesis, Chiral Catalysts, Ligands, and Reagents, Hydroformylation, Landis Ligands, Privileged Ligands and Complexes
相关文献及参考
- 1. Axtell, A.T. et al. Angew. Chem. Int. Ed. Engl. 44 , 5834, (2005) 摘要
- 2. Clark, T.P. et al. J. Am. Chem. Soc. 127 , 5040, (2005) 摘要
