Synthesis and properties of ω-(hydroxyaryl)alkylsulfides based on 2-isobornyl-6-methyl-4-propylphenol

Proceeding from 2-isobornyl-6-methyl-4-propylphenol new derivatives have been synthesized having sulfur atoms included in different functional groups. Antiradical and antioxidant activity, as well as membrane-protecting properties of the derivatives of 2-isobornyl-6-methyl-4-propylphenol in chemical and biological model systems have been investigated.     

Synthesis and evaluation of the antioxidant properties for some novel aminomethyl derivatives of 2,6-diisobornylphenol bearing a pinane moiety

Some new derivatives based on 2,6-diisobornylphenol and containing amine moieties of the pinane structure at the para-position relative to the phenolic hydroxy group were synthesized. The antioxidant properties of the obtained compounds were estimated using various in vitro models. The introduction of diamine moiety into a starting molecule led to a significant increase in the radical scavenging activity and the ability to chelate Fe²⁺ ions.

     

Synthesis oftertiaryamidomethyl derivatives of 2-isobornyl-4-methylphenol

Derivatives containing tertiary amidomethyl groups were prepared by reaction of a secondary aminomethyl derivative of 2-isobornyl-4-methylphenol with succinic and phthalic anhydrides and (1S)-camphanic acid chloride.     

Resolution of racemic 2-isobornyl-4-methylphenol into enantiomers

Resolution of racemic 2-isobornyl-4-methylphenol into enantiomers was performed following its transformation into diastereomers by the reaction with (1S)-camphanoyl chloride.     

Asymmetrically substituted tetra(meso-aryl)porphyrins bearing peripheral 2,6-diisobornylphenol and 2,6-di-tert-butylphenol moieties

Russian Chemical Bulletin - Asymmetrically substituted tetra(meso-aryl)porphyrins bearing peripheral diisobornyl- phenol and di-tert-butylphenol moieties were synthesized by a mixed aldehyde...     

Oxidation of substituted phenols with chlorine dioxide

Chlorine dioxide was used to oxidize sterically hindered phenols and their derivatives (2,6-di-tertbutylphenol, 2,6-diisobornylphenol, 2,6-di-tert-butyl-4-methylphenol, 2,6-diisobornyl-4-methylphenol, and 3,5-diisobornyl-4-hydroxybenzaldehyde) in organic solvent.     

Composition and properties of the reaction products of p-cresol with camphene

Russian Chemical Bulletin - The products of the reaction between p-cresol and camphene were isolated and characterized. Their antiradical activity and toxicity were studied. The pharmacological...