84459-43-8Relevant academic research and scientific papers
The autorecycling oxidation of benzylamine by synthetic 8-hydroxy-5-deazaflavin derivatives
Hirayama,Kawase,Kimachi,Tanaka,Yoneda
, p. 1255 - 1259 (2007/10/02)
Various 8-hydroxy-5-deazaflavin derivatives were synthesized as the model compounds of coenzyme F420. These compounds oxidized benzylamine to benzaldehyde more efficiently than the corresponding 8-unsubstituted 5-deazaflavin.
A New, General, and Convenient Synthesis of 5-Deazaflavins (5-Deazaisoalloxazines) and Bis-(5-deazaflavin-10-yl)alkanes
Nagamatsu, Tomohisa,Hashiguchi, Yuko,Yoneda, Fumio
, p. 561 - 565 (2007/10/02)
The condensation of 6-substituted aminouracils or bis(uracil-6-amino)alkanes with o-halogenobenzaldehydes in dimethylformamide led to the formation of the corresponding 5-deazaflavins or bid(5-deazaflavin-10-yl)alkanes in a single step.
A New, General, and Convenient Synthesis of 5-Deazaflavins (5-Deazaisoallooxazines)
Nagamatsu, Tomohisa,Hashigushi, Yuko,Higuchi, Masatsugu,Yoneda, Fumio
, p. 1085 - 1086 (2007/10/02)
The condensation of 6-substituted-aminouracils with o-halogenobenzaldehydes in dimethylformamide led to the formation of the corresponding 5-deazaflavins in a single step.
