116128-29-1 | Diacetato[(R)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II)

Packsize	Purity	Availability	Price	Discounted Price
200mg	97%	in stock	$57.00	$40.00

Description

• Catalog Number: AA14984
• Chemical Name: Diacetato[(R)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II)
• CAS Number: 116128-29-1
• Molecular Formula: C52H46O4P2Ru
• Molecular Weight: 897.9368
• MDL Number: MFCD09753021
• SMILES: Cc1ccc(cc1)P(c1ccc2c(c1c1c(ccc3c1cccc3)P(c1ccc(cc1)C)c1ccc(cc1)C)cccc2)c1ccc(cc1)C.[O-]C(=O)C.[O-]C(=O)C.[Ru+2]

Upstream Synthesis Route

The Diacetato[(R)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) complex is a versatile catalyst commonly employed in chemical synthesis. With its unique structure and properties, this catalyst plays a crucial role in facilitating various organic transformations.One prominent application of this ruthenium complex is in asymmetric hydrogenation reactions. Asymmetric hydrogenation is a key process in organic chemistry for the selective reduction of unsaturated compounds such as ketones, imines, and enamides. The Diacetato[(R)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) catalyst, with its chiral ligands, enables the synthesis of enantiomerically pure compounds, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals.Additionally, this ruthenium catalyst is utilized in carbon-carbon bond formation reactions, including asymmetric allylic substitutions and allylic alkylation. These transformations are vital in the construction of complex molecular structures with high stereocontrol, making the Diacetato[(R)-(+)-2,2'-bis(di-p-tolylphosphino)-1,1'-binaphthyl]ruthenium(II) catalyst a preferred choice for synthetic chemists aiming to access chiral compounds efficiently and selectively.