Oxidative two-way regiocontrolled coupling of 3-methoxycarbonylcatechol and indoles to arylindoles
Yoshinari Sawama1, Shoko Kuwata2, Miyu Mae1
1Graduate School of Pharmaceutical Sciences, Osaka University, 1-6, Yamada-oka, Suita, Osaka 565-0871, Japan. sawama@phs.osaka-u.ac.jp.
Abstract:
3-Methoxycarbonylcatechol effectively underwent two-way regiocontrolled coupling with indoles via an ortho-benzoquinone intermediate, resulting from phenyliodine(III) diacetate oxidation, to generate 4-adducts or 5-adducts with or without BF3·Et2O in a one-pot manner. DFT calculations confirmed the obtained regioselectivities.
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