Abstract
AbstractIn this work, carbazoles, one of the most important types of nitrogenous compounds, were used as substrates to synthesize dicarbazolyl(aryl)methanols in moderate to excellent yields (up to 95%). This simple and efficient strategy can regioselectively form an sp3 quaternary carbon with two large sterically hindered carbazole rings, one benzene ring, and an active hydroxy group in a one-pot reaction. The resulting triarylmethanes are all new products, and have high potential as building blocks for medicinal chemistry or materials science.
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