Some scientific research about 221012-82-4

After consulting a lot of data, we found that this compound(221012-82-4)Application of 221012-82-4 can be used in many types of reactions. And in most cases, this compound has more advantages.

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, Synthesis called Synthesis of homoallylic alcohols via Lewis acid assisted enantioselective desymmetrization, Author is Yu, Bing; Menard, Frederic; Isono, Naohiro; Lautens, Mark, the main research direction is butenediol carbonate arylboronate enantioselective allylic substitution rhodium catalyst; homoallylic alc asym synthesis.Application of 221012-82-4.

A highly enantioselective allylic substitution of (Z)-but-2-ene-1,4-diol derivatives was developed using a Rh(I) catalyst and arylboronates as nucleophiles. The reaction yields versatile homoallylic alcs. from readily available linear bis-carbonates.

After consulting a lot of data, we found that this compound(221012-82-4)Application of 221012-82-4 can be used in many types of reactions. And in most cases, this compound has more advantages.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider