Arylspiroborates derived from 4-tert-butylcatechol and 3,5-di-tert- butylcatechol and their antimicrobial activities

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

doi:10.1002/jhet.1997

Arylspiroborates derived from 4-tert-butylcatechol and 3,5-di-tert- butylcatechol and their antimicrobial activities

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

Research output: Contribution to journal › Article › peer-review

9 Scopus citations

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.

Original language	English
Pages (from-to)	157-161
Number of pages	5
Journal	Journal of Heterocyclic Chemistry
Volume	51
Issue number	1
DOIs	https://doi.org/10.1002/jhet.1997
State	Published - Jan 2014
Externally published	Yes

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Webb, M. I., Halcovitch, N. R., Bowes, E. G., Lee, G. M., Geier, M. J., Vogels, C. M., O'Neill, T., Li, H., Flewelling, A., Decken, A., Gray, C. A., & Westcott, S. A. (2014). Arylspiroborates derived from 4-tert-butylcatechol and 3,5-di-tert- butylcatechol and their antimicrobial activities. Journal of Heterocyclic Chemistry, 51(1), 157-161. https://doi.org/10.1002/jhet.1997

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title = "Arylspiroborates derived from 4-tert-butylcatechol and 3,5-di-tert- butylcatechol and their antimicrobial activities",

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.",

author = "Webb, \{Michael I.\} and Halcovitch, \{Nathan R.\} and Bowes, \{Eric G.\} and Lee, \{Graham M.\} and Geier, \{Michael J.\} and Vogels, \{Christopher M.\} and Taryn O'Neill and Haoxin Li and Andrew Flewelling and Andreas Decken and Gray, \{Christopher A.\} and Westcott, \{Stephen A.\}",

year = "2014",

month = jan,

doi = "10.1002/jhet.1997",

language = "English",

volume = "51",

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journal = "Journal of Heterocyclic Chemistry",

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AU - Webb, Michael I.

AU - Halcovitch, Nathan R.

AU - Bowes, Eric G.

AU - Lee, Graham M.

AU - Geier, Michael J.

AU - Vogels, Christopher M.

AU - O'Neill, Taryn

AU - Li, Haoxin

AU - Flewelling, Andrew

AU - Decken, Andreas

AU - Gray, Christopher A.

AU - Westcott, Stephen A.

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AB - 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.

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JF - Journal of Heterocyclic Chemistry

IS - 1

ER -

Arylspiroborates derived from 4-tert-butylcatechol and 3,5-di-tert- butylcatechol and their antimicrobial activities

Abstract

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