All Stories

  1. Reaction of Tertiary 2‐Chloroketones with Cyanide Ions: Application to 3‐Chloroquinolinediones
  2. Preparation of compounds including quinoline-2,4-dione and 1,2,3-triazolyl moieties in molecules.
  3. Synthesis of Bis(1,2,3-Triazole) Functionalized Quinoline-2,4-Diones
  4. 4-Hydroxyquinolin-2-one and Quinoline-2,4-dione based Compounds
  5. Design, synthesis and antitubercular potency of 4-hydroxyquinolin-2(1 H )-ones
  6. Synthesis of 1,4-Benzodiazepine-2,5-diones by Base Promoted Ring Expansion of 3-Aminoquinoline-2,4-diones
  7. Fischer indolisation of N-(α-ketoacyl)anthranilic acids.
  8. Oxidative ring opening of 3-hydroxyquinoline-2,4(1H,3H)-diones into N-(α-ketoacyl)anthranilic acids
  9. 4-Hydroxy-1-methyl-3-phenylquinolin-2(1H)-one
  10. 3-Ethyl-3-hydroxy-8-methoxyquinoline-2,4(1H,3H)-dione monohydrate
  11. 3-Ethyl-4-hydroxy-8-methoxyquinolin-2(1H)-one
  12. 2-Hydroxy-2-methyl-1-phenylindolin-3-one
  13. Copper(I)-Catalyzed [ 3+ 2] Cycloaddition of 3-Azidoquinoline-2,4(1H,3H)-diones with Terminal Alkynes
  14. 3-Ethyl-8-methoxy-4-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)quinolin-2(1H)-one
  15. Selective formation of glycosidic linkages of N-unsubstituted 4-hydroxyquinolin-2-(1H)-ones
  16. The first entry to pyrrolo[2,3-c]quinoline-2,4(3aH,5H)-diones
  17. Rearrangement of furo[2,3-c]quinoline-2,4(3aH,5H)-diones to furo[3,4-c]quinoline-3,4(1H,5H)-diones
  18. Limitations of the Wittig–Horner-type annulation of fluorobutenolide moiety to 3-hydroxyquinoline-2,4(2H,3H)-diones. Novel modifications of the Perkow reaction including fluorinated acyloxy leaving groups
  19. Formation and structure elucidation of two novel spiro[2H-indol]-3(1H)-ones
  20. Reaction of malonates with camphoranile synthesis of 4-hydroxy-2-pyridones attached to the bornane ring system
  21. Pyran-2-ones as Synthons for Pyridazine-3-carboxylic Derivatives. Oxidation of Nitrogen-Rich Compounds
  22. New modification of the Perkow reaction: halocarboxylate anions as leaving groups in 3-acyloxyquinoline-2,4(1H,3H)-dione compounds
  23. Synthesis of highly symmetric mesomeric triazaphenalene betaines
  24. Efficiency of some novel carbon black/rubber coupling agents
  25. Thermal Rearrangement of 3-Hydroxy-1H,3H-quinoline-2,4-diones to 3-Acyloxy-2,3-dihydro-1H-indol-2-ones
  26. Syntheses of 3-Aminoquinoline- 2,4(1H,3H)-diones
  27. Novel Ring Contraction of 3-Hydroxy-2,4(1H,3H)-quinolinediones in Aqueous Alkali. The First Convenient Route to 2-Hydroxyindoxyls
  28. A New Transformation of 2H-Pyran-2-one ring: First Synthesis of Pyridazino[4,3-c]azepines and their Oxidation with Thallium(III) Nitrate or Copper(II) Acetate
  29. Conversion of 3-hydroxy-1,2,3,4-tetrahydroquinoline-2,4-diones to 2,3a,4,5-tetrahydrofuro[2,3-c]quinoline-2,4-dionesviaan intramolecular wittig reaction
  30. Synthesis of 4-hydroxy-2(1H)-pyridones from azomethines and substituted dialkylmalonates
  31. Reaction of 3-hydroxy-1,2,3,4-tetrahydroquinoline-2,4-diones with ethyl(triphenylphosphoranylidene)acetate
  32. N-(2-Methyl-2-nitropropyl) and N-Nitroso Derivatives of Some Diamines
  33. Synthesis and Some Reactions of 3-Substituted 1,4-Bis(4-hydroxy-2-oxo-1,2-dihydroquinolin-6-yloxy)butanes
  34. Amination of naphthoquinones with azidotrimethylsilane
  35. Hydroboration of 1-(5-hexenyl)piperidine and trans–1-(3-hexenyl)piperidine
  36. Hydroboration of N,N-dimethyl(2-vinylbenzyl)amine
  37. Hydroboration of 1-allyl-1,2,3,4-tetrahydroquinoline
  38. Hydroboration of 1,4-diallylpiperazine
  39. Syntheses of piperazines substituted on the nitrogen atoms with allyl, propyl, 2-hydroxypropyl and 3-hydroxypropyl groups
  40. Hydroboration of 1-(3-butenyl)piperidine and 1-(4-pentenyl)piperidine
  41. On hydroboration of 2-allyl-1,2,3,4-tetrahydroisoquinoline
  42. The synthesis of some alcohols derived from 1,2,3,4-tetrahydroisoquinoline and from 1,2,3,4-tetrahydroquinoline
  43. Syntheses of some ω-(1,2,3,6-tetrahydro-1-pyridyl)-1-alkanols
  44. Hydroboration of N-allyl derivatives of pyrrolidine, piperidine, hexahydroazepine and morpholine
  45. Reaction of 1-pyridyl-1,3-butanediones and 1,3-dipyridyl-1,3-propanediones