Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Conference, General Review, e-EROS Encyclopedia of Reagents for Organic Synthesis called 3,3′-Bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3R)-; 3,3′-Bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3S)-, Author is Srinivasarao, Madduri, which mentions a compound: 221012-82-4, SMILESS is COC(C=C1P(C2=CC=CC=C2)C3=CC=CC=C3)=NC(OC)=C1C4=C(OC)N=C(OC)C=C4P(C5=CC=CC=C5)C6=CC=CC=C6, Molecular C38H34N2O4P2, Related Products of 221012-82-4.
Properties and applications of 3,3′-bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3R)-; 3,3′-bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3S)-, a chiral biaryl bisphosphine ligands used for high activity and selectivity in catalytic hydrogenation of ketones, β-ketoesters, α,β-unsaturated carbonyl compounds, quinolines; transfer hydrogenation, Pauson-Khand-type reactions, carbonylation and other reductions are reviewed.
From this literature《3,3′-Bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3R)-; 3,3′-Bipyridine, 4,4′-bis(diphenylphosphino)-2,2′,6,6′-tetramethoxy-, (3S)-》,we know some information about this compound(221012-82-4)Related Products of 221012-82-4, but this is not all information, there are many literatures related to this compound(221012-82-4).
Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider