Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/13562

TitleEnzymatic synthesis of Tinuvin
Author(s)Schroeder, M.
Pereira, Luciana
Rodríguez Couto, S.
Erlacher, Angelika
Schoening, K.-U.
Paulo, Artur Cavaco
Guebitz, G. M.
KeywordsLaccase
Oxidative coupling
Tinuvin
Trametes hirsuta
Biotransformation
Issue dateJun-2007
PublisherElsevier
JournalEnzyme and Microbial Technology
Abstract(s)Coupling of 3-(3-tert-butyl-4-hydroxyphenyl) propionic acid methylester to 1H-benzotriazole using a laccase from Trametes hirsuta was studied. The potentially resulting coupling product Tinuvin 1130 is an important UV-absorber used in polymer based materials. Oxidation of the phenol by the laccase led to homomolecular coupling reactions while the laccase did not attack 1H-benzotriazole. Due to the homomolecular reaction of the phenol in the presence of laccase coupling of phenol and 1H-benzotriazole was only observed when 1H-benzotriazole was applied in four-fold molar excess. The reaction was monitored by UV/vis spectroscopy, TLC and MS (ion trap) analysis. Coupling of 1H-benzotriazole took place in ortho position according to the postulated mechanism.
TypeArticle
URIhttp://hdl.handle.net/1822/13562
DOI10.1016/j.enzmictec.2006.11.026
ISSN0141-0229
Publisher versionhttp://www.sciencedirect.com/science/article/pii/S0141022906005850
Peer-Reviewedyes
AccessOpen access
Appears in Collections:DET/2C2T - Artigos em revistas internacionais com arbitragem científica

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