4.5 Article

The synthesis of xanthones, xanthenediones, and spirobenzofurans: Their antibacterial and antifungal activity

期刊

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
卷 21, 期 23, 页码 7085-7088

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bmcl.2011.09.088

关键词

Synthesis; Xanthones; Xanthenediones; Spirobenzofurans; Antimicrobial activity

资金

  1. SABINA (Southern African Biochemistry and Informatics for Natural Products Network)
  2. National Research Foundation (NRF) [GUN 2053652]
  3. RDP of the NRF (South Africa)
  4. Research Niche
  5. Pretoria
  6. University of the Witwatersrand (Science Faculty Research Council)

向作者/读者索取更多资源

Exposure of the phenol, (5-bromo-2-hydroxyphenyl)(2,4,5-trimethoxyphenyl)methanone 18 to ceric ammonium nitrate (CAN) resulted in the formation of 7-bromo-3,4a-dimethoxy-2H-xanthene-2,9( 4aH)-dione 19 and 5-bromo-2',5'-dimethoxy-3H-spiro[benzofuran-2,1'-cyclohexa[2,5]diene]-3,4'-dione 20. The brominated spirobenzofuran 20 was then subjected to Suzuki-Miyaura reactions to give six derivatives 22a-f. These compounds, related diones and xanthones displayed mostly noteworthy antimicrobial activity, particularly towards the yeasts Cryptococcus neoformans and Candida albicans. Diones 15 and 30 displayed significant activity (7.8 mu g/mL) against C. albicans and C. neoformans, respectively. Furthermore, dione 10 displayed the most significant activity (3.6 mu g/mL) against both yeasts. (C) 2011 Elsevier Ltd. All rights reserved.

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