Supporting Information
Supporting Information File 1: Graphical representation of QS activity of natural and α-haloacylated analogues. | ||
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Supporting Information File 2: 1H and 13C NMR data and spectra, IR, HRMS, optical rotation and melting point data, chromatographic separation and yields of synthesized compounds. | ||
Format: PDF | Size: 2.9 MB | Download |
Cite the Following Article
Synthesis and biological evaluation of novel N-α-haloacylated homoserine lactones as quorum sensing modulators
Michail Syrpas, Ewout Ruysbergh, Christian V. Stevens, Norbert De Kimpe and Sven Mangelinckx
Beilstein J. Org. Chem. 2014, 10, 2539–2549.
https://doi.org/10.3762/bjoc.10.265
How to Cite
Syrpas, M.; Ruysbergh, E.; Stevens, C. V.; De Kimpe, N.; Mangelinckx, S. Beilstein J. Org. Chem. 2014, 10, 2539–2549. doi:10.3762/bjoc.10.265
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