75427-52-0Relevant 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.
Donator-substituted 5-Deazaflavins, II: Hydroxy- and 8-Dimethylamino-5-deazaflavins - Model Compounds of Naturally Occuring (Deaza-)Flavocoenzyms
Grauert, Rolf W.
, p. 937 - 950 (2007/10/02)
Donator-substituted 5-deazaflavins 7 were prepared by a Vilsmeier procedure from the anilinouracil derivatives 5 via 6 as stable intermediates.Spectroscopic comparison of the 5-deazaflavins 7 shows, that resonance of the substituents increases in the sequ
A Novel Synthesis of Pyrimidoquinoline-2(3H),4(10H)-diones (5-Deazaflavins) and Analogues by the Oxidative Cyclization of 5,5'-Arylmethylenebis-(6-alkylamino-3-methyluracils)
Yoneda, Fumio,Mori, Kenya,Sakuma, Yoshiharu,Yamaguchi, Hiroyuki
, p. 978 - 981 (2007/10/02)
The oxidative coupling of 5,5'-arylmethylenebis-(6-alkylamino-3-methyluracils), prepared by the condensation of 6-alkylamino-3-methyluracils and arenecarbaldehydes, with diethyl azodiformate afforded the corresponding pyrimidoquinoline-2(3H),4(10H)
