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Arylspiroborates Derived from 4‐ tert ‐Butylcatechol and 3,5‐Di‐ tert ‐butylcatechol and Their Antimicrobial Activities
Author(s) -
Webb Michael I.,
Halcovitch Nathan R.,
Bowes Eric G.,
Lee Graham M.,
Geier Michael J.,
Vogels Christopher M.,
O'Neill Taryn,
Li Haoxin,
Flewelling Andrew,
Decken Andreas,
Gray Christopher A.,
Westcott Stephen A.
Publication year - 2014
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.1997
Subject(s) - chemistry , potassium hydroxide , boron , alkali metal , boric acid , potassium , medicinal chemistry , antimicrobial , single crystal , organic chemistry , crystallography
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