All Stories

  1. Synthesis and antibacterial activity of novel N -acylsulfonamides
  2. A one-pot three-component synthesis of novel α-sulfamidophosphonates under ultrasound irradiation and catalyst-free conditions
  3. A novel, rapid and green method of phosphorylation under ultrasound irradiation and catalyst free conditions
  4. A greener procedure for the synthesis of α-ureidophosphonates under ultrasound irradiation. An X-ray crystallographic study
  5. Convenient Synthesis of Novel N-Acylsulfonamides Containing Phosphonate Moiety
  6. Synthesis and antibacterial activity of sulfonamides. SAR and DFT studies
  7. Efficient Synthesis, Characterization, and Antibacterial Activity of Novel N-Acylsulfonamides and Sulfonylureas
  8. ChemInform Abstract: A Simple, Rapid, and Efficient N‐Boc Protection of Amines under Ultrasound Irradiation and Catalyst‐Free Conditions.
  9. Cytotoxic study of three derivatives amidophosphonates on alternative cellular model: Paramecium tetraurelia
  10. An Efficient Method for the Synthesis of Novel N-acylsulfonamides Using Tin (IV) Chloride as Catalysts
  11. A simple and eco-sustainable method for the sulfonylation of amines under microwave-assisted solvent-free conditions
  12. A New, Efficient, and Catalyst-free Microwave-assisted Approach for Formation of O-tert-Butoxy Carbonates
  13. Host–guest interaction between 3,4-dihydroisoquinoline-2(1H)-sulfonamide and β-cyclodextrin: Spectroscopic and molecular modeling studies
  14. A simple, rapid, and efficient N-Boc protection of amines under ultrasound irradiation and catalyst-free conditions
  15. Synthesis and Biological Activity of New ChiralN-Acylsulfonamide Bis-oxazolidin-2-ones
  16. A simple and eco-sustainable method for theO-Boc protection/deprotection of various phenolic structures under water-mediated/catalyst-free conditions
  17. Synthesis and structural study of N-acetyl-1,2,3,4-tetrahydroisoquinoline-2-sulfonamide obtained using H6P2W18O62 as acidic solid catalyst
  18. Efficient Synthesis of Modified Sulfamides and Cyclosulfamides Containing Phosphonate Moieties
  19. Synthesis and structural study of new substituted chiral sulfamoyl oxazolidin-2-ones
  20. Efficient deprotection of Boc group in amines and sulfamides using Dawson heteropolyacid catalyst
  21. Efficient Method for the Synthesis of Diazaphospholidines: Toxicological Evaluation
  22. Efficient Method for The Synthesis of α-Amidophosphonates via the Michaelis-Arbuzov Reaction
  23. A Simple and Efficient Green Method for the Deprotection of N-Boc in Various Structurally Diverse Amines under Water-mediated Catalyst-free Conditions
  24. N-tert-Butoxycarbonylation of Structurally Diverse Amines and Sulfamides under Water-Mediated Catalyst-Free Conditions
  25. Toxic effects of phosphoramidate onParameciumsp. with special emphasis on respiratory metabolism, growth, and generation time
  26. Effect of novel phosphoramidate on growth and respiratory metabolism of Paramecium aurelia
  27. (4S)-4-Benzyl-N-{[(4S)-4-benzyl-2-oxo-1,3-oxazolidin-3-yl]sulfonyl}-2-oxo-1,3-oxazolidine-3-carboxamide
  28. Crystal Structure of 4-Phenyl-piperazine-1-sulfonamide
  29. ChemInform Abstract: A New Sulfa‐Heterocyclic Compounds Containing Aziridine Moiety, 3‐Benzyl‐2‐thia‐1,3‐diazabicyclo[3.1.0]hexane 2,2‐Dioxide (II) and Its Reaction with Nucleophiles.
  30. ChemInform Abstract: New Pseudonucleosides Containing Chiral Oxazolidin‐2‐ones and Cyclosulfamides as Aglycones: Synthesis and Antiviral Evaluation
  31. 1,2,3,4-Tetrahydroisoquinoline-2-sulfonamide
  32. A New Sulfa-Heterocyclic Compounds Containing Aziridine Moiety, 3-Benzyl-2-thia-1,3-diazabicyclo[3.1.0]hexane 2,2-Dioxide and Its Reaction with Nucleophiles
  33. New Pseudonucleosides Containing Chiral Oxazolidin-2-Ones andCyclosulfamidesas Aglycones: Synthesis and Antiviral Evaluation
  34. Efficient Synthesis of Chiral 1,1′‐Sulfonyl Bisaziridines.
  35. Efficient Synthesis of Chiral 1,1′‐Sulfonyl Bisaziridines
  36. Cyclosulfamides as Constraint Dipeptides: The Synthesis and Structure of Chiral Substituted 1,2,5-Thiadiazolidine 1,1-Dioxides: Evaluation of the Toxicity
  37. Simple and Efficient Synthesis of New Chiral N,N′‐Sulfonyl Bis‐oxazolidin‐2‐ones.
  38. Simple and efficient synthesis of new chiral N,N′‐sulfonyl bis‐oxazolidin‐2‐ones
  39. N‐Chlorosulfonyloxazolidin‐2‐ones: Synthesis, Structure, and Reactivity Toward Aminoesters
  40. N‐Chlorosulfonyloxazolidin‐2‐ones: Synthesis, Structure, and Reactivity Toward Aminoesters.
  41. Simple and Efficient Cleavage Reaction of the Boc Group in Heterocyclic Compounds.
  42. Simple and efficient cleavage reaction of the boc group in heterocyclic compounds
  43. Synthesis of New Pseudonucleosides Containing Chiral Cyclosulfamides as Agycone
  44. Synthesis of New Pseudonucleosides Containing ChiralCyclosulfamidesas Agycone
  45. Synthese et N-Acylation Regiospecifique de 1,2,5-Thiadiazolidines 1,1-Dioxydes Chirales
  46. Synthèse Et Cyclisation De Carboxylsulfamides Dérivés D'amines Et D'α-Hydroxyesters. Éavaluation De L'Activité Bactéeriostatique