New learning discoveries about 591-12-8

As far as I know, this compound(591-12-8)Related Products of 591-12-8 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 5-Methylfuran-2(3H)-one, is researched, Molecular C5H6O2, CAS is 591-12-8, about Inverse-Electron-Demand Palladium-Catalyzed Asymmetric [4+2] Cycloadditions Enabled by Chiral P,S-Ligand and Hydrogen Bonding, the main research direction is enantioselective diastereoselective inverse electron demand palladium catalyzed cycloaddition; chiral phosphorus sulfur ligand palladium catalyzed asym cycloaddition; hydrogen bonding palladium catalyzed asym cycloaddition; P,S ligand; cycloaddition; heterocycles; hydrogen bonding; palladium.Related Products of 591-12-8.

Catalytic asym. cycloadditions of ambident Pd-containing dipolar species with nucleophilic dipolarophiles, namely, inverse-electron-demand cycloadditions, are challenging and underdeveloped. Possibly, the inherent linear selectivity of Pd-catalyzed intermol. allylations and the lack of efficient chiral ligands are responsible for this limitation. Herein, two cycloadditions of such intermediates with deconjugated butenolides and azlactones were accomplished by using a novel chiral hybrid P,S-ligand and hydrogen bonding [e.g., vinyl carbamate I + butenolide II → dihydroquinol-2-one III (92%, 93% ee, >95:5 d.r.)]. By doing so, highly functionalized, optically active dihydroquinol-2-ones were produced with generally high reaction efficiencies and selectivities. Preliminary DFT calculations were performed to explain the high enantio- and diastereoselectivities.

As far as I know, this compound(591-12-8)Related Products of 591-12-8 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Reference:
Pyrimidine | C4H4N2 – PubChem,
Pyrimidine – Wikipedia