64338-22-3Relevant academic research and scientific papers
Improved synthesis of tocopherol fatty alcohols and analogs: microglial activation modulators
Muller, Thierry,Coowar, Djalil,Hanbali, Mazen,Heuschling, Paul,Luu, Bang
, p. 12025 - 12040 (2006)
The synthesis of tocopherol fatty alcohols (TFAs), potent microglial activation modulators, was achieved via C-alkylation of trimethylhydroquinone. Several analogs, in particular water-soluble prodrugs, have been synthesized using a Wittig reaction and th
Radical scavenging activity and performance of novel phenolic antioxidants in oils during storage and frying
Catel, Yohann,Aladedunye, Felix,Przybylski, Roman
scheme or table, p. 55 - 66 (2012/03/27)
Novel phenolic antioxidants: 2a (6′-hydroxy-2′,5′, 7′,8′-tetramethylchroman-2′-yl)methyl 3-methoxy-4- hydroxycinnamate, 2b (6′-hydroxy-2′,5′,7′,8′- tetramethylchroman-2′-yl)methyl 3,5-dimethoxy-4-hydroxycinnamate, 2c (6′-hydroxy-2′,5′,7′,8′-tetramethylchr
Synthesis, radical scavenging activity, protection during storage, and frying by novel antioxidants
Catel, Yohann,Aladedunye, Felix,Przybylski, Roman
scheme or table, p. 11081 - 11089 (2011/06/21)
Novel antioxidants, derivatives of trolox, and selected phenolic acids have been prepared in good yields and fully characterized by 1H NMR, 13C NMR, and MS. Their antioxidant activities have been assessed by DPPH and ORAC assays, and during frying and accelerated storage tests. Novel phenolic compounds exhibited higher radical scavenging activities than both trolox and R-tocopherol. Trolox hydroxybenzoate showed a significantly higher protection than R-tocopherol under storage conditions. All new antioxidants performed better than R-tocopherol under frying conditions. Moreover, their outstanding thermal stability makes them more valuable than R-tocopherol for frying applications.
