
A series of new 2,3-disubstituted-3,4-dihydro-2H-1,3-benzoxazines were prepared in moderate to excellent yields by aza-acetalizations of aromatic aldehydes with 2-(N-substituted aminomethyl)phenols in the presence of TMSCl. Their structures were confirmed by IR, 1H-NMR, 13C-NMR, MS and elemental analysis. The fungicidal activities of the target compounds were preliminarily evaluated, and some compounds exhibited good activity against Rhizoctonia solani.
fungicidal activity, Antifungal Agents, Magnetic Resonance Spectroscopy, synthesis, chlorotrimethylsilane, Fungi, Organic chemistry, Microbial Sensitivity Tests, Article, Benzoxazines, QD241-441, 2,3-disubstituted-1,3-benzoxazine
fungicidal activity, Antifungal Agents, Magnetic Resonance Spectroscopy, synthesis, chlorotrimethylsilane, Fungi, Organic chemistry, Microbial Sensitivity Tests, Article, Benzoxazines, QD241-441, 2,3-disubstituted-1,3-benzoxazine
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