作者:Alessandra Napolitano、Alessandro Pezzella、Marco d'Ischia、Giuseppe Prota
DOI:10.1016/0040-4039(96)00806-4
日期:1996.6
Oxidation of 5,6-dihydroxy-2,3-dimethylindole (1) with NaIO4 or o-chloranil afforded a yellow transient intermediate with λmax around 360 nm which was identified as the hitherto unknown 2,3-dimethyl-5,6-indolequinone (2) by straightforward 1H-NMR analysis.
5,6-二羟基-2,3-二甲基吲哚(氧化1)用的NaIO 4或ö -chloranil得到黄色瞬态与中间λ最大周围360纳米,其被鉴定为迄今未知的2,3-二甲基-5,6- -吲哚醌(2)通过简单的1 H-NMR分析。