Archives for Chemistry Experiments of 221012-82-4

Compound(221012-82-4)Product Details of 221012-82-4 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound((R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine), if you are interested, you can check out my other related articles.

The three-dimensional configuration of the ester heterocycle is basically the same as that of the carbocycle. Compound: (R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine(SMILESS: 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,cas:221012-82-4) is researched.HPLC of Formula: 138984-26-6. The article 《Enantioselective bis-alkoxycarbonylation of styrene catalyzed by novel chiral dipyridylphosphine cationic palladium(II) complexes》 in relation to this compound, is published in Journal of Molecular Catalysis A: Chemical. Let’s take a look at the latest research on this compound (cas:221012-82-4).

The preparation of new palladium complexes that are composed of a series of chiral dipyridylphosphines have been described. The structure of the complex [{(R)-1}Pd(H2O)2](OTf)2 was unambiguously determined by single-crystal X-ray diffractometry. These complexes were found to be effective in the asym. bis-methoxycarbonylation of styrene, reaching up to 84% e.e. and 79% chemoselectivity for dimethyl-2-phenylsuccinate (DMPS) under the optimal conditions. In addition, the complexes exhibited almost identical enantioselectivity on DMPS.

Compound(221012-82-4)Product Details of 221012-82-4 received a lot of attention, and I have introduced some compounds in other articles, similar to this compound((R)-2,2′,6,6′-Tetramethoxy-4,4′-bis(diphenylphosphino)-3,3′-bipyridine), if you are interested, you can check out my other related articles.

Reference:
Quinoxaline – Wikipedia,
Quinoxaline | C8H6N2 | ChemSpider