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Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities

Research output: Contribution to journalJournal articlepeer-review

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  • Michael I. Webb
  • Nathan R. Halcovitch
  • Eric G. Bowes
  • Graham M. Lee
  • Michael J. Geier
  • Christopher M. Vogels
  • Taryn O'Neill
  • Haoxin Li
  • Andrew Flewelling
  • Andreas Decken
  • Christopher A. Gray
  • Stephen A. Westcott
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<mark>Journal publication date</mark>01/2014
<mark>Journal</mark>Journal of Heterocyclic Chemistry
Issue number1
Volume51
Number of pages5
Pages (from-to)157-161
Publication StatusPublished
Early online date23/10/13
<mark>Original language</mark>English

Abstract

A family of arylspiroborates has been prepared by the addition of either 4-tert-butylcatechol or 3,5-di-tert-butylcatechol to boric acid and an alkali metal hydroxide. All compounds were characterized fully using multinuclear NMR spectroscopy and by elemental analyses. A single crystal X-ray diffraction was carried out on potassium (bis-(3,5-di-tertbutyl[1,2-benzenediolato(2-)-O,O]borate)) (8). All compounds displayed appreciable anti-microbial activities.