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2 e for an alternative mechanism, resulting in autoxidative cyclization of the heptadienone moiety as a
3 on of aldehyde 9 during desilylation through autoxidative decarbonylation afforded benzophenone 2b, d
4 products of 1-bromo-2,3-dimethylbenzene, and autoxidative degradation of phenyl-di-tert-butylphosphin
7 the AGE-modified protein residues indicated autoxidative glycosylation, but not glycoxidation, as th
11 c phenol precursor l-dopa were compared with autoxidative processes and quantitatively assessed by ox