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Building trans-bicyclo[4.4.0]decanes/decenes in complex multifunctional frameworks: the case for antibiotic development

期刊

NATURAL PRODUCT REPORTS
卷 38, 期 5, 页码 880-889

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d0np00052c

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资金

  1. National Science Foundation [CHE1531620, CHE2003692]
  2. National Institute of General Medical Sciences [GM119426]
  3. Royal Society of New Zealand Te Aparangi for a Rutherford Foundation Postdoctoral Fellowship
  4. Kate Edger Educational Charitable Trust
  5. Maurice Wilkins Centre for Molecular Biodiscovery
  6. New Zealand Ministry of Business, Innovation and Employment [5000449]

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This article discusses the research on natural products containing trans-Bicyclo[4.4.0]decane/decene structures in antibacterial activity from 2000 to 2020, emphasizing the special strategies required in their construction process.
Covering: 2000 to 2020. trans-Bicyclo[4.4.0]decane/decene (such as trans-decalin and trans-octalin)-containing natural products display a wide range of structural diversity and frequently exhibit potent and selective antibacterial activities. With one of the major factors in combatting antibiotic resistance being the discovery of novel scaffolds, the efficient construction of these natural products is an attractive pursuit in the development of novel antibiotics. This highlight aims to provide a critical analysis on how the presence of dense architectural and stereochemical complexity necessitated special strategies in the synthetic pursuits of these natural trans-bicyclo[4.4.0]decane/decene antibiotics.

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