| Literature DB >> 22514188 |
Pijus K Sasmal1, Susana Carregal-Romero, Alice A Han, Craig N Streu, Zhijie Lin, Kazuhiko Namikawa, Samantha L Elliott, Reinhard W Köster, Wolfgang J Parak, Eric Meggers.
Abstract
In the quest for the identification of catalytic transformations to be used in chemical biology and medicinal chemistry, we identified iron(III) meso-tetraarylporphines as efficient catalysts for the reduction of aromatic azides to their amines. The reaction uses thiols as reducing agents and tolerates water, air, and other biological components. A caged fluorophore was employed to demonstrate that the reduction can be performed even in living mammalian cells. However, in vivo experiments in nematodes (Caenorhabditis elegans) and zebrafish (Danio rerio) revealed a limitation to this method: the metabolic reduction of aromatic azides.Entities:
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Year: 2012 PMID: 22514188 DOI: 10.1002/cbic.201100719
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164