Some scientific research about 221012-82-4

As far as I know, this compound(221012-82-4)Formula: C38H34N2O4P2 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, Research Support, Non-U.S. Gov’t, Organic Letters called Kinetic Resolution of 2-Substituted 2,3-Dihydro-4-pyridones by Palladium-Catalyzed Asymmetric Allylic Alkylation: Catalytic Asymmetric Total Synthesis of Indolizidine (-)-209I, Author is Lei, Bai-Lin; Zhang, Qing-Song; Yu, Wei-Hua; Ding, Qiu-Ping; Ding, Chang-Hua; Hou, Xue-Long, the main research direction is dihydropyridone palladium PPhos asym allylic alkylation kinetic resolution catalyst; allyl dihydropyridone stereoselective preparation; indolizidine 209I total synthesis.Formula: C38H34N2O4P2.

The kinetic resolution of 2-substituted-2,3-dihydro-4-pyridones was realized via a Pd-catalyzed allylic substitution reaction using a com. available (S)-P-Phos as a ligand, affording optically active dihydropyridones and C-allylated dihydropyridones in high yields and good enantioselectivities with the S-factor up to 43. With this protocol, a catalytic asym. total synthesis of indolizidine (-)-209I (I) was realized for the first time.

As far as I know, this compound(221012-82-4)Formula: C38H34N2O4P2 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