Eric Brustad

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Name: Brustad, Eric
Organization: University of North Carolina at Chapel Hill , USA
Department:
Title: Assistant(PhD)
Co-reporter:Adrienne L. Snyder ; Eric M. Brustad
ChemBioChem 2014 Volume 15( Issue 12) pp:1731-1733
Publication Date(Web):
DOI:10.1002/cbic.201402210
Co-reporter:Joshua G Gober, Eric M Brustad
Current Opinion in Chemical Biology (December 2016) Volume 35() pp:
Publication Date(Web):1 December 2016
DOI:10.1016/j.cbpa.2016.09.004
•There is a need for the development of novel biocatalysts for reactions not found in Nature.•Heme proteins can catalyze non-native carbenoid-mediated and nitrenoid-mediated transformations.•Non-native activity and selectivity of heme proteins can be improved using protein engineering.Despite increasing interest in using enzymes as tools for synthesis, many reactions discovered through the creativity of synthetic chemists remain beyond the scope of biocatalysis. This vacancy in the field has compelled researchers to develop strategies to adapt protein scaffolds for new reactivity. Heme proteins have recently been shown to activate synthetic precursors to generate reactive metallocarbenoid and metallonitrenoid species that enable the biosynthetic construction of novel C–C, C–N, and other bonds using mechanisms not previously explored by Nature. By interrogating heme proteins with synthetic, non-natural reagents, scientists are merging the reaction space traditionally dominated by organocatalysis and transition metal catalysis with the mild reaction conditions, selectivity, and adaptability imparted by native protein scaffolds.
Cyclopropanecarboxylic acid, 2-phenyl-, ethyl ester, (1S,2R)-
Cyclopropanecarboxylic acid, 2-phenyl-, ethyl ester, (1R,2S)-
Ferrate(2-), [3,7,12,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-κN21,κN22,κN23,κN24]-, hydrogen (1:2), (SP-4-2)-
Ferrate(2-), [7,12-diethenyl-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-κN21,κN22,κN23,κN24]-, hydrogen (1:2), (SP-4-2)-