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Structure of 911415-22-0
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This sterically hindered phosphine ligand features two electron-rich aryl groups flanking a chiral propanediyl backbone, enabling robust coordination in palladium-catalyzed cross-coupling reactions. The bulky tert-butyl substituents enhance stability and prevent undesired decomposition pathways under standard conditions.
1,1'-[(1S,3S)-1,3-dimethyl-1,3-propanediyl]bis[1,1-bis[4-(1,1-dimethylethyl)phenyl]-phosphine] serves as a sterically hindered, bench-stable phosphine ligand that facilitates palladium-catalyzed cross-coupling reactions. Its bis(tert-butyl)aryl substitution enhances oxidative stability and promotes efficient catalyst turnover in Suzuki-Miyaura and Negishi couplings. The chiral propanediyl backbone provides controlled spatial orientation, improving selectivity in asymmetric transformations. This ligand enables high-yielding reactions under mild conditions with broad functional group tolerance.
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Lot numbers can be found on the outside label of a product: