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Sulfides, sulfones, and sulfoxides of the furan-2(5H)-one series. synthesis and structureA number of 4- and 5-R-sulfanylfuran-2(5H)-one derivatives were synthesized, and their oxidation
Sulfides, sulfones, and sulfoxides of the furan-2(5H)-one series. synthesis and structureA number of 4- and 5-R-sulfanylfuran-2(5H)-one derivatives were synthesized, and their oxidation
Stereochemical Features of the Crystallization of Eight-Membered 1,5-Diazaheterocycles with Chiral Aminoindanole Fragments at Nitrogen Atoms
Unrecognized Cycloaddition Reactions of N-Alkyl-α,β-Unsaturated Imines Occurring in Biosystems and Their Biological Roles
Unrecognized Cycloaddition Reactions of N-Alkyl-α,β-Unsaturated Imines Occurring in Biosystems and Their Biological Roles
"Lp⋯synthon" interaction as a reason for the strong amplification of synthon-forming hydrogen bonds of the interactions is characterized by quantum-chemistry models using R. Bader's theory (QTAIM), the values
Targeting Bacillus cereus cells: Increasing efficiency of antimicrobials by the bornyl-possessing 2(5H)-furanone derivative bactericidal effects against Gram-positive bacteria. Here we report that 3,4-dichloro-5(S)-[(1S,2R,4S)-1
Unraveling the molecular mechanism of selective antimicrobial activity of 2(5H)-furanone derivative against Staphylococcus aureus native and 2D PAGE, we confirm that F105 changes the charge of some proteins by either oxidation
Antimicrobial effects of sulfonyl derivative of 2(5H)-furanone against planktonic and biofilm associated methicillin-resistant and -susceptible Staphylococcus aureus, we describe a novel 3-chloro-5(S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-4
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