R. Teixeira, J. L. Pereira, S. F. D. Silva
Mar 5, 2014
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Influential Citations
10
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Journal
Journal of Molecular Structure
Abstract
Abstract Two hydroxylated isobenzofuranones 3 and 4 were synthesized from benzoic acids. The compounds were fully characterized by IR, NMR ( 1 H and 13 C), HRMS, and X-ray crystallography. Compounds 3 and 4 crystallized in the space group Pc and P2 1 /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.