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Results 1 - 4 of 4
EC Number Substrates Commentary Substrates Organism Products Commentary (Products) Reversibility
Display the reaction diagram Show all sequences 1.14.20.11(2S)-3-(1H-indol-3-yl)-2-isocyanopropanoate + 2-oxoglutarate + O2 - Fischerella ambigua 3-[(Z)-2-isocyanoethenyl]-1H-indole + succinate + 2 CO2 + H2O - ?
Display the reaction diagram Show all sequences 1.14.20.11(2S)-3-(1H-indol-3-yl)-2-isocyanopropanoate + 2-oxoglutarate + O2 - Fischerella ambigua UTEX 1903 3-[(Z)-2-isocyanoethenyl]-1H-indole + succinate + 2 CO2 + H2O - ?
Display the reaction diagram Show all sequences 1.14.20.11more enzyme initiates stereoselective olefination via a benzylic C-H bond activation by an Fe(IV)-oxo intermediate, and the reaction likely proceeds through a radical- or carbocation-induced decarboxylation to complete C=C bond installation Fischerella ambigua ? - ?
Display the reaction diagram Show all sequences 1.14.20.11more enzyme initiates stereoselective olefination via a benzylic C-H bond activation by an Fe(IV)-oxo intermediate, and the reaction likely proceeds through a radical- or carbocation-induced decarboxylation to complete C=C bond installation Fischerella ambigua UTEX 1903 ? - ?
Results 1 - 4 of 4