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![(−)-Bis[(S)-1-phenylethyl]amine (CAS 56210-72-1) - chemical structure image](https://media.scbt.com/product/minus-bis-s-1-phenylethyl-amine-56210-72-1-structure_09_10_t_91058.jpg "Molecular structure of (−)-Bis[(S)-1-phenylethyl]amine, CAS Number: 56210-72-1")
(−)-Bis[(S)-1-phenylethyl]amine (CAS 56210-72-1)
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(−)-Bis[(S)-1-phenylethyl]amine, a chiral diamine compound, functions as a ligand in asymmetric catalysis. (−)-Bis[(S)-1-phenylethyl]amine acts as a chiral auxiliary in various organic reactions, facilitating the formation of enantiomerically pure products. The amine group of the compound interacts with the substrate, forming a complex that allows for selective and efficient transformation of the reactants. (−)-Bis[(S)-1-Phenylethyl]Amine′s mechanism of action involves coordinating with metal catalysts to form a chiral environment, which directs the stereochemistry of the reaction. By serving as a chiral template, (−)-Bis[(S)-1-phenylethyl]amine enables the synthesis of complex molecules with high enantioselectivity, making it useful in the development of chiral compounds.
(−)-Bis[(S)-1-phenylethyl]amine (CAS 56210-72-1) References
- (R)-2,2'-BINAPHTHOYL-(S,S)-DI(1-PHENYLETHYL) AMINOPHOSPHINE. SCALABLE PROTOCOLS FOR THE SYNTHESES OF PHOSPHORAMIDITE (FERINGA) LIGANDS. | Smith, CR., et al. 2008. Organic Synth. 85: 238-247. PMID: 19655040
- Optimisation of a lithium magnesiate for use in the non-cryogenic asymmetric deprotonation of prochiral ketones. | Francos, J., et al. 2014. Dalton Trans. 43: 1408-12. PMID: 24201759
- Desymmetrization Approach to the Synthesis of Optically Active P-Stereogenic Phosphin-2-en-4-ones. | Łastawiecka, E., et al. 2021. J Org Chem. 86: 6195-6206. PMID: 33900770
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
(−)-Bis[(S)-1-phenylethyl]amine, 1 g | sc-234086 | 1 g | $47.00 |