Supporting Information
| Supporting Information File 1: Synthetic procedure of 1, UV, IR, 1H NMR, 13C NMR, COSY, HSQC, HMBC spectra for natural and synthetic 1, and UV, IR, 1H NMR, 13C NMR spectra for synthetic intermediates. | ||
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Cite the Following Article
4-Hydroxy-3-methyl-2(1H)-quinolone, originally discovered from a Brassicaceae plant, produced by a soil bacterium of the genus Burkholderia sp.: determination of a preferred tautomer and antioxidant activity
Dandan Li, Naoya Oku, Yukiko Shinozaki, Yoichi Kurokawa and Yasuhiro Igarashi
Beilstein J. Org. Chem. 2020, 16, 1489–1494.
https://doi.org/10.3762/bjoc.16.124
How to Cite
Li, D.; Oku, N.; Shinozaki, Y.; Kurokawa, Y.; Igarashi, Y. Beilstein J. Org. Chem. 2020, 16, 1489–1494. doi:10.3762/bjoc.16.124
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- Coulon, P. M. L.; Zlosnik, J. E. A.; Déziel, E. Presence of the Hmq System and Production of 4-Hydroxy-3-Methyl-2-Alkylquinolines Are Heterogeneously Distributed between Burkholderia cepacia Complex Species and More Prevalent among Environmental than Clinical Isolates. Microbiology spectrum 2021, 9, e0012721. doi:10.1128/spectrum.00127-21
- Saalim, M.; Villegas-Moreno, J.; Clark, B. R. Bacterial Alkyl-4-quinolones: Discovery, Structural Diversity and Biological Properties. Molecules (Basel, Switzerland) 2020, 25, 5689. doi:10.3390/molecules25235689
