123557-14-2Relevant academic research and scientific papers
Synthesis of bifunctionalised flavins for incorporation into well defined redox systems
Edwards, Timothy R. G.,Gani, David
, p. 935 - 956 (1990)
The syntheses of isoalloxazines functionalised at C-7 and N-3, suitable for two point parallel face attachment to gold in the construction of flavin-gold electrodes, are described.
Synthesis of Multifunctional 2-Aminobenzimidazoles on DNA via Iodine-Promoted Cyclization
Fan, Jing,Feng, Jing,Franklin, G. Joseph,Lancia, David R.,Li, Jin,Liu, Guansai,O'connell, Jonathan,Peng, Ting,Su, Liqiang,Wan, Jinqiao
supporting information, (2020/02/13)
2-Aminobenzimidazole cores are among the most common structural components in medicinal chemistry and can be found in many biologically active molecules. Herein, we report a mild protocol for the synthesis of multifunctional 2-aminobenzimidazoles on-DNA with broad substrate scopes. The reaction conditions expand our ability to design and synthesize 2-aminobenzimidazole core-focused DNA-encoded libraries.
Construction of a Stable Flavin-Gold Electrode displaying Very Fast Electron Transfer Kinetics
Edwards, Timothy R. G.,Cunnane, Vincent J.,Parsons, Roger,Gani, David
, p. 1041 - 1043 (2007/10/02)
The bis-phenylthiourea phenethylisoalloxazine (6) was synthesised and was attached to the gold through its thiourea side-chains; cyclic voltammetric investigation of the redox properties of the system confirmed that the flavin was a stable adsorbed species and revealed that electron transfer between the conductor and the flavin was very fast.
