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- Hydrophilic oxygen radical absorbance capacity values of low-molecular-weight phenolic compounds containing carbon, hydrogen, and oxygen. Shuhei Sakurai, Akito Kikuchi, Hiroaki Gotoh
, RSC Adv.
, 2022
, 12
, 4094
- 433. Alkylperoxy-radicals. Part II. Kinetics of autoxidations retarded by 2 : 4 : 6-trialkylphenols. A. F. Bickel, E. C. Kooyman
, J. Chem. Soc.
, 1956
, 2215
- Chi-MIC-share: a new feature selection algorithm for quantitative structure–activity relationship models. Yuting Li, Zhijun Dai, Dan Cao, Feng Luo, Yuan Chen, Zheming Yuan
, RSC Adv.
, 2020
, 10
, 19852
- Decomposition of organic hydroperoxides. Part 5.—Decomposition of tert-butyl hydroperoxide catalyzed by nitriles and base. H. Berger
, Trans. Faraday Soc.
, 1962
, 58
, 1137
- Installing a functional group into the inactive ω-chain end of PMMA and PS-b-PMMA by terminal-selective transesterification. Kohei Yoshida, Takuya Yamamoto, Kenji Tajima, Takuya Isono, Toshifumi Satoh
, Polym. Chem.
, 2019
, 10
, 3390
- Some products formed from phenolic inhibitors during the autoxidation of cumene. R. F. Moore, William A. Waters
, J. Chem. Soc.
, 1954
, 243
- 315. The constitution of ψ-santonin. A correction to part III. Wesley Cocker, Cyril Lipman, D. R. A. Whyte
, J. Chem. Soc.
, 1950
, 1519
- The use of the tertiary alkyl tetraoxide–peroxyl equilibrium, ROOOOR ⇌ 2RO2˙, as a clean source of tertiary alkyl peroxyls. James D. Honeywill, Brynmor Mile
, J. Chem. Soc., Perkin Trans. 2
, 2002
, 569