dc.contributor.author |
Wellington, Kevin W
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dc.contributor.author |
Steenkamp, P
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dc.contributor.author |
Brady, D
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dc.date.accessioned |
2010-08-25T13:46:55Z |
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dc.date.available |
2010-08-25T13:46:55Z |
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dc.date.issued |
2010-02 |
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dc.identifier.citation |
Wellington, KW, Steenkamp, P, and Brady, D. 2010. Diamination by n-coupling using a commercial laccase. Bioorganic and Medicinal Chemistry, Vol. 18, pp 1406–1414 |
en |
dc.identifier.issn |
0968-0896 |
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dc.identifier.uri |
http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6TF8-4Y6450C-2-H&_cdi=5220&_user=958262&_pii=S0968089610000465&_orig=search&_coverDate=02/15/2010&_sk=999819995&view=c&wchp=dGLzVtb-zSkWb&md5=ec57bc8b705cf6773909443f2c699a0e&ie=/sdarticle.pdf
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dc.identifier.uri |
http://hdl.handle.net/10204/4212
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dc.identifier.uri |
https://www.sciencedirect.com/science/article/pii/S0968089610000465
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dc.identifier.uri |
https://doi.org/10.1016/j.bmc.2010.01.025
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dc.identifier.uri |
https://www.sciencedirect.com/science/article/pii/S0968089610000465
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dc.description |
Copyright: 2010 Elsevier. This is the author's accepted manuscript, the definitive version is published in the Bioorganic and Medicinal Chemistry Journal, Vol. 18(4), pp 1406–1414 |
en |
dc.description.abstract |
Nuclear diamination of p-hydrobenzoquinones with aromatic and aliphatic primary amines was catalyzed by a immobilised commercial laccase, Denilite II Base, from Novozymes. The amine and the p-hydrobenzoquinone was reacted under mild conditions (at room temperature and at 35oC in a reaction vessel open to air in the presence of laccase and a co-solvent to afford, exclusively, the diaminated pbenzoquinone. These compounds may have potential antiallergic, antibiotic, anticancer, antifungal, antiviral and 5-lipoxygenase inhibiting activity. |
en |
dc.language.iso |
en |
en |
dc.publisher |
Elsevier |
en |
dc.subject |
P-hydrobenzoquinones |
en |
dc.subject |
Green chemistry |
en |
dc.subject |
P-benzoquinones |
en |
dc.subject |
Biocatalysis |
en |
dc.subject |
Laccase |
en |
dc.subject |
Denilite base |
en |
dc.subject |
Oxidative enzymes |
en |
dc.title |
Diamination by n-coupling using a commercial laccase |
en |
dc.type |
Article |
en |
dc.identifier.apacitation |
Wellington, K. W., Steenkamp, P., & Brady, D. (2010). Diamination by n-coupling using a commercial laccase. http://hdl.handle.net/10204/4212 |
en_ZA |
dc.identifier.chicagocitation |
Wellington, Kevin W, P Steenkamp, and D Brady "Diamination by n-coupling using a commercial laccase." (2010) http://hdl.handle.net/10204/4212 |
en_ZA |
dc.identifier.vancouvercitation |
Wellington KW, Steenkamp P, Brady D. Diamination by n-coupling using a commercial laccase. 2010; http://hdl.handle.net/10204/4212. |
en_ZA |
dc.identifier.ris |
TY - Article
AU - Wellington, Kevin W
AU - Steenkamp, P
AU - Brady, D
AB - Nuclear diamination of p-hydrobenzoquinones with aromatic and aliphatic primary amines was catalyzed by a immobilised commercial laccase, Denilite II Base, from Novozymes. The amine and the p-hydrobenzoquinone was reacted under mild conditions (at room temperature and at 35oC in a reaction vessel open to air in the presence of laccase and a co-solvent to afford, exclusively, the diaminated pbenzoquinone. These compounds may have potential antiallergic, antibiotic, anticancer, antifungal, antiviral and 5-lipoxygenase inhibiting activity.
DA - 2010-02
DB - ResearchSpace
DP - CSIR
KW - P-hydrobenzoquinones
KW - Green chemistry
KW - P-benzoquinones
KW - Biocatalysis
KW - Laccase
KW - Denilite base
KW - Oxidative enzymes
LK - https://researchspace.csir.co.za
PY - 2010
SM - 0968-0896
T1 - Diamination by n-coupling using a commercial laccase
TI - Diamination by n-coupling using a commercial laccase
UR - http://hdl.handle.net/10204/4212
ER -
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en_ZA |