-Oxidation of 4-methylpyrrole-2-carboxylates with DDQ in the presence of a glycol proceeded smoothly on the methyl group at the C4 position regioselectively to afford the corresponding pyrrole-2,4-dicarboxylates directly.Direct oxidation of a methyl group of 2,4,6-trimethylphenol and 3-methyl-9H-carbazole into carboxylates was also demonstrated.
(MS WordStyle "04 Het-Abstract") 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) is a highly effective oxidant widely used in organic synthesis and its major functions include dehydrogenation, such as aromatization of hydroaromatic compounds, introduction of a double bond into carbonyl compounds, and oxidation of alcohols.Benzylic oxidation with DDQ in the presence of oxygen nucleophiles gives the corresponding oxygen-functionalized compounds. Furthermore, alternative oxidative cyclization and coupling reactions have been also reported.
1,2During our investigation on the syntheses of phytochromobilin (PΦB), phycocyanobilin (PCB), biliverdin (BV) and their analogs including sterically locked derivatives toward elucidation of the structure and function of phytochromes, 3 oxidative functionalization of pyrroles by the use of quinones was explored.In the case that DDQ was used as an oxidant, the α-position of the alkyl substituent at the C4 position was regioselectively oxidized in the presence of AcOH to afford 4-(1-acetoxyalkyl)pyrrole derivatives.In contrast, the corresponding 4-acylpyrroles were produced when MeOH was used instead of AcOH as a