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作 者:Daniel Teoh Chuan Tan Hasnah Osman Suriyati Mohamad Azlina Harun Kamaruddin
机构地区:[1]School of Chemical Sciences, Universiti Sains Malaysia, Minden 11800, Penang, Malaysia [2]School of Biological Sciences, Universiti Sains Malaysia, Minden 11800, Penang, Malaysia [3]School of Chemical Engineering, Universiti Sains Malaysia, Nibong Tebal 14300, Penang, Malaysia
出 处:《Journal of Chemistry and Chemical Engineering》2012年第1期84-89,共6页化学与化工(英文版)
摘 要:Nitro and halogen substituted derivatives of the juglone naphthoquinone were synthesized and assayed for their antibacterial activity. 8-Nitrojuglone was obtained as the exclusive product from the direct nitration of juglone with nickel (Ⅱ) nitrate and p-toluenesulphonic acid. In addition, a series of five 8-halojuglone derivatives were synthesized via a solvent-free Friedel-Crafts acylation reaction. One of the acylation reactions afforded an anthraquinone-type derivative as the minor product. The 8-nitrojuglone derivative displayed the most notable activity against S. aureus. However, all of the 8-halojuglone derivatives were found to be less active than juglone against the bacteria assayed.
关 键 词:NAPHTHOQUINONE NITRATION Friedel-Crafts acylation ANTHRAQUINONE antibacterial activity.
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