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dc.creatorTeixeira, R. R.-
dc.creatorPereira, J. L.-
dc.creatorSilva, S. F. da-
dc.creatorGuilardi, S.-
dc.creatorPaixão, D. A.-
dc.creatorAnconi, C. P. A.-
dc.creatorAlmeida, W. B. de-
dc.creatorEllena, J.-
dc.creatorForlani, G.-
dc.identifier.citationTEIXEIRA, R. R. et al. Synthesis, characterization and phytotoxic activity of hydroxylated isobenzofuran-1(3H)-ones. Journal of Molecular Structure, Amsterdam, v. 1061, p. 61-68, 5 Mar. 2014.pt_BR
dc.description.abstractwo hydroxylated isobenzofuranones 3 and 4 were synthesized from benzoic acids. The compounds were fully characterized by IR, NMR (1H and 13C), HRMS, and X-ray crystallography. Compounds 3 and 4 crystallized in the space group Pc and P21/n, respectively. DFT calculations were used to confirm undoubtedly their NMR chemical shifts. Biological assays showed that these compounds are capable of interfering with the radicle growth of monocotyledonous and dicotyledonous species, whereas the photosynthetic electron transport chain was substantially unaffected.pt_BR
dc.sourceJournal of Molecular Structurept_BR
dc.subjectX-ray analysispt_BR
dc.subjectDFT calculationspt_BR
dc.subjectAnálise de raios-Xpt_BR
dc.subjectCálculos DFTpt_BR
dc.titleSynthesis, characterization and phytotoxic activity of hydroxylated isobenzofuran-1(3H)-onespt_BR
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