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Williams, W., Dunk, T., Landerkin, K., Smith, E., White, V., Salomon, J. and Reuben, J. (2005) Accuracy of Identification in BD Phoenix? Using the New Low Inoculum Mode. As presented at the 105th General Meeting of the American Society for Microbiology.
https://www.bd.com/ds/technicalCenter/whitepapers/lr884.pdf

has been cited by the following article:

• TITLE: Synthesis of α-Naphthol and 2,4,7-Trimethyl-Quinolin-5-ol by Using Manganese (III) Acetate and Analysis of Its Antimicrobial Properties

  AUTHORS: Gülderen Uysal Akkuş

  KEYWORDS: Manganese (III) Acetate, Biological Activity, Radical Reaction, Aromatic, Ketone

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.6 No.1, March 15, 2016

  ABSTRACT: This study involves the aromatization reactions of some ketone derivatives through Manganese (III) acetate. The ketone derivatives used in the study are α-tetralone (1a), 2,4,7-trimethyl-7,8-dihydro quinolinone (1b). At the end of the aromatization reactions of these ketone derivatives the synthesized structures of α-naphthol (2a), 2,4,7-trimethylquinoline-5-ol (2b) were identified by spectroscopic methods such as IR, 1H-NMR, 13C-NMR, FAB-MS respectively. Micro-organism types such as Escherichia coli, ATCC 25922, Klepsiella pneumoniae, Staphylococcus aureus NRRL B767, Salmonella typhimurium NRRLB 4420, Bacillus subtilis NRS 744, Bacillus cereus ATCC 11778, Micrococcus luteus ATCC-9341, Listeria monoaytopenus ATCC-7644 bacteria and yeast fungus Candida albicans were used to study the anti-microbial properties of the synthesized 2b compound. The obtained results have determined that compound number 2b has a good antibacterial impact on Bacillus subtilis (NRS-744).