Results 41 to 50 of about 6,997 (207)
Synthesis of Some New Enaminoketones, Analogous of Milrinone, 4,Pyrones and Related 4-Pyridones [PDF]
Synthesis of 4-(N,N- dimethylamino)-3-aryl-3-butene-2-one, ethyl-5-aryl-4-oxo-4H-pyran-2-carboxylate, ethyl-5-aryl-4-pyridones-2-carboxylate and 5-aryl-3-cyano-5-methyl-2-pyridones (aryl=3-thienyl, 2-furyl) are described.
Aziz Shahrisa, Salar Hemmati
doaj
Using a combination of metal‐promoted reactivity, in‐situ covalent bond modification, and hydrogen bonding‐promoted fluorine labilization, a unified approach was developed to self‐assemble a library of customizable ligand architectures directly at the nickel center via selective cleavage of C‒F or C‒O bonds and the formation of C‒C or C‒N bonds.
Aleksandr Sorvanov+5 more
wiley +1 more source
Schematic of the working principle of aqueous ZIBs and the benefits of electronic conductive metal–organic frameworks (EC‐MOFs) as cathode materials. ABSTRACT Zinc‐ion batteries (ZIBs) have significant potential for advancements in energy storage systems owing to their high level of safety and theoretical capacity. However, ZIBs face several challenges,
Chuntao Yang, Youlin Xiang, Yingjian Yu
wiley +1 more source
6-Methyl-2-pyridone pentahydrate [PDF]
Crystals of the title compound, C6H7NO·5H2O, were grown over a period of several weeks from an aqueous solution of the commercial compound. The molecule crystallizes in space group P\overline 1 and there are two independent 6-methyl-2-pyridone (Hmhp) molecules in the asymmetric unit, together with ten molecules of water.
Clegg W, Nichol GS
openaire +2 more sources
In the title compound, C21H17N5O3S3·C3H7NO, the toluenesulfonamide ring and the combined ring system involving the pyridone and benzothiazole rings subtend an interplanar angle of 39.86 (4)°.
Rasha A. Azzam+3 more
doaj +1 more source
Is Mycobacterial InhA a Suitable Target for Rational Drug Design?
InhA is the target of isoniazid, a first‐line antituberculosis drug. Isoniazid is, in fact, a prodrug that needs to be activated. Researchers are trying to develop direct inhibitors of InhA. This includes the resolution of crystallographic structures. The Protein Data Bank contains over a hundred InhA structures.
Julien Rizet+7 more
wiley +1 more source
An efficient method for the synthesis of highly substituted bicyclic pyridone derivatives containing the dithiocarbamate group is reported via a one-pot three-component reaction of 2-(alkylthio)thioazlactones, diamines, and nitroketene dithioacetal in ...
Marziyeh Saeedi+6 more
doaj +1 more source
Dysregulated proteolysis mediated by kallikrein‐related peptidases (KLKs) and iron overload are involved in the progression of neurodegenerative diseases. Deferasirox, an clinically‐approved iron chelator, and its newly synthesized derivatives have been identified as inhibitors of major central nervous system KLKs with low cytotoxicity and effective ...
Rilès Boumali+11 more
wiley +1 more source
A two‐stage dication pool strategy using alkenyl thianthrenium intermediates has been developed for anti‐Markovnikov hydrofunctionalization. This method differs from previous approaches in its reaction mechanism and addresses their most significant limitation, namely, the restricted generality of the nucleophile. The approach has been extended to other
Bence Sóvári+7 more
wiley +2 more sources
catena-Poly[[(nitrato-κ2O,O′)silver(I)]-μ3-4-pyridone-κ3O:O:O]
In the title complex, [Ag(NO3)(C5H5NO)]n, the AgI atom is coordinated by two O atoms from two different 4-pyridone ligands and two O atoms from one nitrate anion, displaying a nearly planar coordination geometry.
Xian-Ge Wu, Jun-Xia Xiao, Liang Qin
doaj +1 more source