65331-45-5Relevant academic research and scientific papers
Mild environment-friendly oxidative debenzylation of N-benzylanilines using DMSO as an oxidant
Yoshinaga, Tatsuro,Iwata, Takayuki,Shindo, Mitsuru
supporting information, p. 191 - 194 (2020/02/25)
Oxidative debenzylation of N-benzyl aromatic amines using DMSO as a non-toxic oxidant and catalyzed by TsOH gave Nphenylimines, which were spontaneously hydrolyzed to form anilines and benzaldehydes in good yields. This reaction employs mild, metal-free conditions. The conditions are also suitable for the debenzylation of benzylphenylethers.
Two isolated intermediates of the Tr?ger's base: synthesis and mechanism
Wan, Yu,Yuan, Rui,Zhang, Wei-chao,Shi, Yan-hui,Lin, Wei,Yin, Wei,Bo, Rong-cheng,Shi, Jing-jing,Wu, Hui
experimental part, p. 3405 - 3409 (2010/06/21)
By controlling the amount of catalyst 1-methyl-3-(2-(sulfooxy)ethyl)-1H-imidazol-3-ium chloride, two new intermediates of Tr?ger's bases (11, 1,6-dimethyl-3-(4-methylphenyl)-1,4-dihydroquinazolin-3-ium tetrafluoroborate and 12, 8-methyl-2,5-bis-(4-methylp
