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 Journal, Article, Angewandte Chemie, International Edition called Iridium-catalyzed enantioselective allyl-allylsilane cross-coupling, Author is Hamilton, James Y.; Hauser, Nicole; Sarlah, David; Carreira, Erick M., which mentions a compound: 1265884-98-7, SMILESS is N1(P2OC3=CC=C4C=CC=CC4=C3C5=C6C=CC=CC6=CC=C5O2)C7=CC=CC=C7C=CC8=CC=CC=C81, Molecular C34H22NO2P, Related Products of 1265884-98-7.
An enantioselective allyl-allylsilane cross-coupling involving racemic branched allylic alcs. and allylsilanes was reported. An iridium-(P,olefin) phosphoramidite complex enabled the transformation with high regio- and stereoselectivity under operationally simple conditions. The utility of the coupling was demonstrated in a concise catalytic, enantioselective synthesis of a pyrethroid insecticide protrifenbute. The structure of the compound (3R,4S)-3-methyl-4-(naphthalen-2-yl)hexane-1,6-diol was confirmed by the single crystal x-ray diffraction anal. and its data were deposited at the Cambridge Crystallog. Data Center as supplementary publication number CCDC 1005708.
There is still a lot of research devoted to this compound(SMILES：N1(P2OC3=CC=C4C=CC=CC4=C3C5=C6C=CC=CC6=CC=C5O2)C7=CC=CC=C7C=CC8=CC=CC=C81)Related Products of 1265884-98-7, and with the development of science, more effects of this compound(1265884-98-7) can be discovered.
Reference:
1,3-Benzodioxole – Wikipedia,
Dioxole | C3H4O2 – PubChem