A facile synthetic route was developed to N-dichloroacetyl-2,3- dihydrobenzoxazole derivatives 3 by cycloaddition of 2-amino-phenol (1) with dichloromethane and acylation of the resultant intermediate 2,3- dihydrobenzoxazole 2 with dichloroacetyl chloride. The structures of the compounds were characterized by IR, 1H NMR, and 13C NMR spectroscopy and elemental analysis. The preliminary biological tests showed that products 3 could protect maize against injury caused by acetochlor to some extent. Copyright © by Walter de Gruyter Berlin Boston.
CITATION STYLE
Fu, Y., Li, G. Y., Ye, F., Zhang, S. S., & Gao, S. (2011). Synthesis and biological activity of some novel N-dichloroacetyl-2,3- dihydrobenzoxazole derivatives. Heterocyclic Communications, 17(1–2), 57–60. https://doi.org/10.1515/HC.2011.010
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