Pest Management Science · 2018 · 32 citations · 18 references
AgricultureBotanyPlant SciencesHerbicide ChemistryHerbicide Mode Of ActionPlant BiochemistryHerbicide ScienceHerbicide Structure-activity RelationshipsHerbicide SynthesisSeed Germination InhibitionActivitiesBiological Activity FeaturesBotanical BioassaysBotanical HerbicidesHerbicidal BioassaysHerbicide Toxicity TestingPrivileged StructuresSubstituent Effects On Biological Activity
BACKGROUND: Despite the need to develop new herbicides with different modes of action, due to weed resistance, many important classes of compounds have been studied poorly for this purpose. Benzoxazoles are considered privileged structures because of their biological activities, but their phytotoxic activities have not received a lot of attention until now. RESULTS: Double vinylic substitution reactions were carried out to furnish four 2-nitromethylbenzoxazoles and one oxazolidine. Benzoxazol-2-ylmethanamine was obtained by reduction of compound 3a. These compounds were evaluated for their phytotoxicity in Allium cepa (onion), Solanum lycopersicum (tomato), Cucumis sativus (cucumber) and Sorghum bicolor (sorghum). Comparison with oxazolidine analogue allowed us to understand that the benzoxazolic structure is very important for the herbicidal activity. CONCLUSION: All the synthesized compounds exhibited biological activity on seed germination. The four 2-nitromethylbenzoxazoles showed phytotoxic activity and the 5-chloro-2-(nitromethyl)benzo[d]oxazole (3b) exhibited higher inhibition than the commercial herbicide against all four plant species tested. © 2018 Society of Chemical Industry.
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Christopher D. Cox, Michael J. Breslin, David B. Whitman et al. · Journal of Medicinal Chemistry · 2010 · 370 citations · Full text
Structure of A23187, a divalent cation ionophore
Michael O. Chaney, Paul V. Demarco, Noel D. Jones et al. · Journal of the American Chemical Society · 1974 · 209 citations