A series of electron withdrawing or donating group substituted phenols were chemoselectively arylated with various substituted bromo-nitroarenes using KOtBu at room temperature via an SNAr pathway. The synthesis of natural alkaloids (carbazoles), dibenzofurans, and a biaryl-indole was achieved from the synthesized nitro-biaryl-ols. © The Partner Organisations 2014.
CITATION STYLE
Kumar, A., Yadav, A., Verma, A., Jana, S., Sattar, M., Kumar, S., … Kumar, S. (2014). Chemoselective arylation of phenols with bromo-nitroarenes: Synthesis of nitro-biaryl-ols and their conversion into benzofurans and carbazoles. Chemical Communications, 50(67), 9481–9484. https://doi.org/10.1039/c4cc03090g
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