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

Research output: Contribution to Journal/Magazine › Journal article › peer-review

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Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities. / Webb, Michael I.; Halcovitch, Nathan R.; Bowes, Eric G. et al.
In: Journal of Heterocyclic Chemistry, Vol. 51, No. 1, 01.2014, p. 157-161.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Webb, MI, Halcovitch, NR, Bowes, EG, Lee, GM, Geier, MJ, Vogels, CM, O'Neill, T, Li, H, Flewelling, A, Decken, A, Gray, CA & Westcott, SA 2014, 'Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities', Journal of Heterocyclic Chemistry, vol. 51, no. 1, pp. 157-161. https://doi.org/10.1002/jhet.1997

APA

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-tertbutylcatechol and their antimicrobial activities. Journal of Heterocyclic Chemistry, 51(1), 157-161. https://doi.org/10.1002/jhet.1997

Vancouver

Webb MI, Halcovitch NR, Bowes EG, Lee GM, Geier MJ, Vogels CM et al. Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities. Journal of Heterocyclic Chemistry. 2014 Jan;51(1):157-161. Epub 2013 Oct 23. doi: 10.1002/jhet.1997

Author

Webb, Michael I. ; Halcovitch, Nathan R. ; Bowes, Eric G. et al. / Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities. In: Journal of Heterocyclic Chemistry. 2014 ; Vol. 51, No. 1. pp. 157-161.

Bibtex

@article{971b7000ef624e159d718ea02172f4c6,
title = "Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol 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.",
keywords = "ANTIFUNGAL ACTIVITY, ESTERS, CATIONS, SALTS, ACID",
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",
pages = "157--161",
journal = "Journal of Heterocyclic Chemistry",
issn = "0022-152X",
publisher = "Heterocorporation",
number = "1",

}

RIS

TY - JOUR

T1 - Arylspiroborates derived from 4-tert-Butylcatechol and 3,5-Di-tertbutylcatechol and their antimicrobial activities

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.

PY - 2014/1

Y1 - 2014/1

N2 - 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.

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.

KW - ANTIFUNGAL ACTIVITY

KW - ESTERS

KW - CATIONS

KW - SALTS

KW - ACID

U2 - 10.1002/jhet.1997

DO - 10.1002/jhet.1997

M3 - Journal article

VL - 51

SP - 157

EP - 161

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

SN - 0022-152X

IS - 1

ER -