The mechanistic mode of oxidation of substituted n,n-dimethylanilines, thioanisoles, and methyl phenyl sulfoxides by 5-ethyl-4a-hydroperoxy-3-methyl-lumiflavin (4a-FlEt-OOH)

✍ Scribed by Shigeru Oae; Kaoru Asada; Toshiaki Yoshimura

• Publisher: Elsevier Science
• Year: 1983
• Tongue: French
• Weight: 230 KB
• Volume: 24
• Category: Article
• ISSN: 0040-4039
• DOI: 10.1016/s0040-4039(00)81631-7

✦ Synopsis

In the oxidation 06 the tit_& compoun&, 5-e~hyL-4a-hydtopehoxy-3-me,thyL-Lumi&win (4a-F1Et-OUH), wan dound to be an eleca7tophLL.k oxidant dim&m to m-ckeohopehaxybenzoic acid.