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Das, Debasis, Eser, Bekir E., Han, Jaehong, Sciore, Aaron, Marsh, E. Neil G. (2011) Oxygen-Independent Decarbonylation of Aldehydes by Cyanobacterial Aldehyde Decarbonylase: A New Reaction of Diiron Enzymes. Angewandte Chemie, 123 (31). 7286-7290 doi:10.1002/ange.201101552

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Reference TypeJournal (article/letter/editorial)
TitleOxygen-Independent Decarbonylation of Aldehydes by Cyanobacterial Aldehyde Decarbonylase: A New Reaction of Diiron Enzymes
JournalAngewandte Chemie
AuthorsDas, DebasisAuthor
Eser, Bekir E.Author
Han, JaehongAuthor
Sciore, AaronAuthor
Marsh, E. Neil G.Author
Year2011 (July 25)Volume123
Issue31
PublisherWiley
DOIdoi:10.1002/ange.201101552Search in ResearchGate
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Mindat Ref. ID7316611Long-form Identifiermindat:1:5:7316611:9
GUID0
Full ReferenceDas, Debasis, Eser, Bekir E., Han, Jaehong, Sciore, Aaron, Marsh, E. Neil G. (2011) Oxygen-Independent Decarbonylation of Aldehydes by Cyanobacterial Aldehyde Decarbonylase: A New Reaction of Diiron Enzymes. Angewandte Chemie, 123 (31). 7286-7290 doi:10.1002/ange.201101552
Plain TextDas, Debasis, Eser, Bekir E., Han, Jaehong, Sciore, Aaron, Marsh, E. Neil G. (2011) Oxygen-Independent Decarbonylation of Aldehydes by Cyanobacterial Aldehyde Decarbonylase: A New Reaction of Diiron Enzymes. Angewandte Chemie, 123 (31). 7286-7290 doi:10.1002/ange.201101552
In(2011, July) Angewandte Chemie Vol. 123 (31) Wiley

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Das, Debasis, Eser, Bekir E., Han, Jaehong, Sciore, Aaron, Marsh, E. Neil G. (2011) Oxygen-Independent Decarbonylation of Aldehydes by Cyanobacterial Aldehyde Decarbonylase: A New Reaction of Diiron Enzymes. Angewandte Chemie International Edition, 50 (31). 7148-7152 doi:10.1002/anie.201101552
Das, Debasis, Eser, Bekir E., Han, Jaehong, Sciore, Aaron, Marsh, E. Neil G. (2012) Berichtigung: Oxygen-Independent Decarbonylation of Aldehydes by Cyanobacterial Aldehyde Decarbonylase: A New Reaction of Diiron Enzymes. Angewandte Chemie, 124 (32). 8004 doi:10.1002/ange.201204831
Das, Debasis, Eser, Bekir E., Han, Jaehong, Sciore, Aaron, Marsh, E. Neil G. (2012) Corrigendum: Oxygen-Independent Decarbonylation of Aldehydes by Cyanobacterial Aldehyde Decarbonylase: A New Reaction of Diiron Enzymes. Angewandte Chemie International Edition, 51 (32). 7881 doi:10.1002/anie.201204831
Paul, Bishwajit, Das, Debasis, Ellington, Benjamin, Marsh, E. Neil G. (2013) Probing the Mechanism of Cyanobacterial Aldehyde Decarbonylase Using a Cyclopropyl Aldehyde. Journal Of The American Chemical Society, 135 (14) 5234-5237 doi:10.1021/ja3115949
Li, Ning, Nørgaard, Hanne, Warui, Douglas M., Booker, Squire J., Krebs, Carsten, Bollinger, J. Martin (2011) Conversion of Fatty Aldehydes to Alka(e)nes and Formate by a Cyanobacterial Aldehyde Decarbonylase: Cryptic Redox by an Unusual Dimetal Oxygenase. Journal Of The American Chemical Society, 133 (16) 6158-6161 doi:10.1021/ja2013517
Sciore, Aaron, Su, Min, Koldewey, Philipp, Eschweiler, Joseph D., Diffley, Kelsey A., Linhares, Brian M., Ruotolo, Brandon T., Bardwell, James C. A., Skiniotis, Georgios, Marsh, E. Neil G. (2016) Flexible, symmetry-directed approach to assembling protein cages. Proceedings of the National Academy of Sciences, 113 (31) 8681-8686 doi:10.1073/pnas.1606013113
(2011) Buxing Han. Angewandte Chemie, 123 (21). 4837 doi:10.1002/ange.201102147
(2011) Graphisches Inhaltsverzeichnis: Angew. Chem. 31/2011. Angewandte Chemie, 123 (31). 7069-7083 doi:10.1002/ange.201190062
La Pierre, Henry S., Scheurer, Andreas, Heinemann, Frank W., Hieringer, Wolfgang, Meyer, Karsten (2014) Synthesis and Characterization of a Uranium(II) Monoarene Complex Supported by δ  Backbonding. Angewandte Chemie, 126 (28). 7286-7290 doi:10.1002/ange.201402050
(2011) Younan Xia. Angewandte Chemie, 123 (31). 7092-7093 doi:10.1002/ange.201103048
(2011) Vorschau: Angew. Chem. 31/2011. Angewandte Chemie, 123 (30). 7063 doi:10.1002/ange.201190061
 
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