Abstract
A number of triarylmethanes were prepared, the majority of which are new. One of the aryl groups is a naphthol, 1,3,5-trimethoxybenzene, or resorcinol, or an indole, pyrrole or pyridine ring. Three synthetic routes are described: (1) reaction of a benzhydrol with an electron-rich aromatic compound; (2) direct condensation of benzaldehyde or hydroxybenzaldehydes, with N,N-dimethylaniline or its derivatives and 2-naphthol; and (3) displacement of benzotriazole in benzotriazolyl derivatives by Grignard reagent according to our recently developed benzotriazole methodology. © 1994.
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CITATION STYLE
Muthyala, R., Katritzky, A. R., & Lan, X. (1994). A synthetic study on the preparation of triarylmethanes. Dyes and Pigments, 25(4), 303–324. https://doi.org/10.1016/0143-7208(94)87017-9
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