Continuously updated synthesis method about 221012-82-4

As far as I know, this compound(221012-82-4)Recommanded Product: 221012-82-4 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 221012-82-4, is researched, 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 C38H34N2O4P2Journal, Article, Angewandte Chemie, International Edition called Enantioselective Palladium-Catalyzed Hydrophosphinylation of Allenes with Phosphine Oxides: Access to Chiral Allylic Phosphine Oxides, Author is Yang, Zhiping; Wang, Jun, the main research direction is enantioselective palladium catalyzed hydrophosphinylation allene phosphine oxide; chiral allylic phosphine oxide preparation; aryl oxyallene phosphine oxide enantioselective preparation crystal mol structure; allene; allylic compound; hydrophosphinylation; palladium; synthetic method.Recommanded Product: 221012-82-4.

A Pd-catalyzed hydrophosphinylation of alkyl and aryl-oxyallenes with phosphine oxides has been developed for the efficient and rapid construction of a family of chiral allylic phosphine oxides with a diverse range of functional groups. This methodol. was further applied in the facile construction of chiral 2H-chromene and later stage functionalization of cholesterol.

As far as I know, this compound(221012-82-4)Recommanded Product: 221012-82-4 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider