N 1, N 10-Ethylene-bridged high-potential flavins: synthesis, characterization, and reactivity
WS Li, N Zhang, LM Sayre
Index: Li, Wen-Shan; Zhang, Nanjing; Sayre, Lawrence M. Tetrahedron, 2001 , vol. 57, # 21 p. 4507 - 4522
Full Text: HTML
Citation Number: 31
Abstract
N1, N10-Ethyleneisoalloxazinium chloride and its 8-Cl-, 7-CF3-, and 3-CH3-7-CF3- substituted analogs were synthesized for the purpose of exhibiting thermal reactivity with organic substrates. The new flavins were characterized spectroscopically and electrochemically, and were found to react with amines, thiols, and phenylhydrazine, the latter case exhibiting catalytic aerobic recycling. Reactions of aliphatic benzylic and ...
Related Articles:
[Sasho; Obase; Ichikawa; Kitazawa; Nonaka; Yoshizaki; Ishii; Shuto Journal of Medicinal Chemistry, 1993 , vol. 36, # 5 p. 572 - 579]
845. Tetrahydroquinoxalines. A new route from o-amino-N-2′-hydroxyethylanilines
[Ramage; Trappe Journal of the Chemical Society, 1952 , p. 4406,4408]