Alloxan-(o -amino-anil) as model chromophore for a 10,10a-ring opened intermediate in flavin-dependent dioxygen activation

This publication has 14 references indexed in Scilit:

• On the chemistry of flavin-dependent oxygen activation III. synthesis of 1.10a-dihydroflavin and its 10.10-aring opened derivative as model chromophores for enzyme-bound intermediates
  Tetrahedron Letters, 1980
• ON THE CHEMISTRY OF FLAVIN DEPENDENT OXYGEN ACTIVATION
  Published by Elsevier ,1979
• The structure of σ‐complexes between flavinium salts and methoxide as revealed by ¹³C nuclear magnetic resonance
  Recueil des Travaux Chimiques des Pays-Bas, 1978
• FLAVIN‐O₂ INTERACTION MECHANISMS AND THE FUNCTION OF FLAVIN IN HYDROXYLATION REACTIONS
  Annals of the New York Academy of Sciences, 1973
• Bacterial bioluminescence - identification of fatty acid as product, its quantum yield and a suggested mechanism
  Biochemical and Biophysical Research Communications, 1973
• Heterocyclic compounds from alloxan and amines. XIII. Phenazine freeradical betaines and their dehydro dimers derived from alloxan and 2-aminodiphenylamines
  Australian Journal of Chemistry, 1971
• Heterocyclic compounds from alloxan and amines. XII. Tetrahydroquinoxalinespirobarbituric acids and 5-(1-Benzimidazolio)-4-barbiturates from 2-Dialkylaminoanilines
  Australian Journal of Chemistry, 1970
• Heterocyclic compounds from alloxan and amines. XI. Uramils, dialuric acids, and related compounds
  Australian Journal of Chemistry, 1970
• 682. The structures of some supposed azetid-2 : 4-diones. Part III. The “alloxan-5-o-dimethylaminoanil” of Rudy and Cramer, and its alkali hydrolysis product
  Journal of the Chemical Society, 1951
• The Preparation of Riboflavin.¹ III. The Synthesis of Alloxazines and Isoalloxazines
  Journal of the American Chemical Society, 1945