Site-Selective Synthesis of 15N- and 13C-Enriched Flavin Mononucleotide Coenzyme Isotopologues
Author:
Affiliation:
1. Department of Chemistry, University of Utah, 315 South 1400 East, Salt Lake City, Utah 84112, United States
Funder
National Institute of General Medical Sciences
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b00640
Reference35 articles.
1. Flavin coenzymes: at the crossroads of biological redox chemistry
2. Edwards, A. M.InFlavins and Flavoproteins: Methods and Protocols, Methods in Molecular Biology;Weber, S.; Schleicher, E., Eds.Springer Science + Business Media:New York, 2014; Vol.1146, pp3–14.
3. The Chemical and Biological Versatility of Riboflavin
4. Briggs, W. R.InFlavins: Photochemistry and Photobiology;Silva, E.; Edwards, A. M., Eds.RSC:Cambridge, 2006; pp183–216.
5. Flavin-mediated dual oxidation controls an enzymatic Favorskii-type rearrangement
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