meso-Bromination of cyano- and aquacobalamins facilitates their processing into Co(II)-species by glutathione
Author:
Funder
Russian Science Foundation
Publisher
Springer Science and Business Media LLC
Subject
Inorganic Chemistry,Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s00775-023-02009-x.pdf
Reference43 articles.
1. Dereven’kov IA, Salnikov DS, Silaghi-Dumitrescu R, Makarov SV, Koifman OI (2016) Redox chemistry of cobalamin and its derivatives. Coord Chem Rev 309:68–83. https://doi.org/10.1016/j.ccr.2015.11.001
2. Salnikov DS, Kucherenko PN, Dereven’kov IA, Makarov SV, van Eldik R (2014) Kinetics and mechanism of the reaction of hydrogen sulfide with cobalamin in aqueous solution. Eur J Inorg Chem. https://doi.org/10.1002/ejic.201301340
3. Salnikov DS, Dereven’kov IA, Artyushina EN, Makarov SV (2013) Interaction of cyanocobalamin with sulfur-containing reducing agents in aqueous solutions. Russ J Phys Chem A 87:44–48. https://doi.org/10.1134/S0036024413010226
4. Dereven’kov IA, Ugodin KA, Makarov SV (2021) Mechanism of the reaction between cyanocobalamin and reduced flavin mononucleotide. Russ J Phys Chem A 95:2020–2024. https://doi.org/10.1134/S003602442110006X
5. Lexa D, Savéant JM, Zickler J (1980) Electrochemistry of vitamin B12. 5. Cyanocobalamins. J Am Chem Soc 102:2654–2663. https://doi.org/10.1021/ja00528a023
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