All Stories

  1. A Glimpse at the Quinoline-Hybridization Approach for the Development of New Antimalarials
  2. Recent developments in biological aspects of chalcones: the odyssey continues
  3. Recent Developments in Intramolecular Cyclization Reactions via Carbon-heteroatom (CX) Bond Formation
  4. Azide–alkyne cycloaddition en route to 4-aminoquinoline–ferrocenylchalcone conjugates: synthesis and anti-TB evaluation
  5. 4-Aminoquinoline-hybridization en route towards the development of rationally designed antimalarial agents
  6. β-Lactam-Synthon-Interceded Facile Synthesis of Functionally Decorated Thiohydantoins
  7. N-Propargylated isatin-Mannich mono- and bis-adducts: Synthesis and preliminary analysis of in vitro activity against Tritrichomonas foetus
  8. ChemInform Abstract: Facile Diastereoselective Synthesis of Functionally Enriched Hydantoins via Base‐Promoted Intramolecular Amidolysis of C‐3 Functionalized Azetidin‐2‐ones.
  9. Synthesis and medicinal chemistry of selected antitubercular natural products and natural product derivatives
  10. Single pot diastereoselective synthesis of six membered cyclic (E)-endo-aldonitrones via intramolecular cyclization of ω-alkenyl oximes
  11. Triflic acid promoted fries rearrangement of C-3 vinyl/isopropenyl-azetidin-2-ones: single-pot synthesis of C-3 functionalized-2-aryl-2,3-dihydro-quinoline-4(1H)-ones
  12. ChemInform Abstract: Diastereoselective Synthesis of 2,3‐Disubstituted 1‐Arylazetidines via NaBH4‐Promoted Facile Reduction of C‐3 Functionalized Azetidin‐2‐ones.
  13. Base-Promoted Expedient Access to Spiroisatins: Synthesis and Antitubercular Evaluation of 1H-1,2,3-Triazole-Tethered Spiroisatin–Ferrocene and Isatin–Ferrocene Conjugates
  14. Facile diastereoselective synthesis of functionally enriched hydantoins via base-promoted intramolecular amidolysis of C-3 functionalized azetidin-2-ones
  15. ChemInform Abstract: Facile, Diastereoselective Synthesis of Functionally Enriched Hexahydroisoquinolines, Hexahydroisoquinolones and Hexahydroisochromones via Inter‐/Intramolecular Amidolysis of C‐3 Functionalized 2‐Azetidinones.
  16. Diastereoselective synthesis of 2,3-disubstituted 1-arylazetidines via NaBH4-promoted facile reduction of C-3 functionalized azetidin-2-ones
  17. ChemInform Abstract: Triflic Acid Mediated Fries Rearrangement of 3‐Dienyl‐azetidinones: Facile Synthesis of 3‐(But‐2‐enylidene)quinolin‐4(3H)‐ones.
  18. β-Lactam-Synthon-Interceded Synthesis of Isatin-Imidazolidine-2-thione Conjugates with Structural Validation using Molecular Dynamic Simulations and Cytotoxic Evaluation
  19. Facile, diastereoselective synthesis of functionally enriched hexahydroisoquinolines, hexahydroisoquinolones and hexahydroisochromones via inter-/intramolecular amidolysis of C-3 functionalized 2-azetidinones
  20. ChemInform Abstract: Synthetic Studies on the Role of Substituents at C‐3 Position on C3—C4 Bond Cleavage of β‐Lactam Ring: Convenient Route for Diastereoselective Synthesis of Pyridin‐2‐ones.
  21. 1H-1,2,3-Triazole-Tethered Isatin–Ferrocene and Isatin–Ferrocenylchalcone Conjugates: Synthesis and in Vitro Antitubercular Evaluation
  22. ChemInform Abstract: β‐Lactam‐Synthon‐Interceded Diastereoselective Synthesis of Functionally Enriched Thioxo‐imidazolidines, Imidazolidin‐2‐ones, Piperazine‐5,6‐diones and 4,5‐Dihydroimidazoles.
  23. Azide–alkynecycloadditionen route towards 1H-1,2,3-triazole-tethered β-lactam–ferrocene and β-lactam–ferrocenylchalcone conjugates: synthesis and in vitro anti-tubercular evaluation
  24. Synthesis of novel 1H-1,2,3-triazole tethered C-5 substituted uracil–isatin conjugates and their cytotoxic evaluation
  25. β-Lactam-synthon-interceded diastereoselective synthesis of functionally enriched thioxo-imidazolidines, imidazolidin-2-ones, piperazine-5,6-diones and 4,5-dihydroimidazoles
  26. ChemInform Abstract: Synthesis, Docking and in vitro Antimalarial Evaluation of Bifunctional Hybrids Derived from β‐Lactams and 7‐Chloroquinoline Using Click Chemistry.
  27. Synthesis and in vitro anti-tubercular evaluation of 1,2,3-triazole tethered β-lactam–ferrocene and β-lactam–ferrocenylchalcone chimeric scaffolds
  28. Synthesis, docking and in vitro antimalarial evaluation of bifunctional hybrids derived from β-lactams and 7-chloroquinoline using click chemistry
  29. Synthetic Studies on the Role of Substituents at C-3 Position on C3-C4 Bond Cleavage of β-Lactam Ring: Convenient Route for Diastereoselective Synthesis of Pyridin-2-ones
  30. ChemInform Abstract: β‐Lactam Synthon Interceded Diastereoselective Synthesis of Novel Thioxo‐imidazolines: A Convenient Access to Functionally Decorated 4,5‐Dihydroimidazoles.
  31. ChemInform Abstract: Antiplasmodial and Cytotoxicity Evaluation of 3‐Functionalized 2‐Azetidinone Derivatives.
  32. β-Lactam-synthon-interceded diastereoselective synthesis of novel thioxo-imidazolines: a convenient access to functionally decorated 4,5-dihydro-imidazoles
  33. Pyrimidine and Imidazole
  34. ChemInform Abstract: Diastereoselective Approach to Novel Octahydroisoquinolones and an Extension to Its One‐Pot Synthesis.
  35. Mercury(II) ion recognition by newly synthesized oxadiazaphosphepine based receptors: coated graphite and polymeric membrane electrodes
  36. Diastereoselective approach to novel octahydroisoquinolones and an extension to its one-pot synthesis
  37. ChemInform Abstract: A Regio‐ and Diastereoselective Transformation of 3‐Dienyl‐2‐azetidinones to Novel Pyrroloxazine.
  38. A regio and diastereoselective transformation of 3-dienyl-2-azetidinones to novel pyrroloxazine
  39. Synthetic medicinal chemistry of selected antimalarial natural products
  40. ChemInform Abstract: Effect of Varying the Anionic Component of a Copper(I) Catalyst on Homologation of Arylacetylenes to Allenes by the Mannich Reaction.
  41. Meclonazepam analogues as potential new antihelmintic agents
  42. Lewis Acid Promoted Aza Diels—Alder Reactions of Acyclic Unactivated 5‐Dienyl Pyrimidinones with N‐Arylimines: Synthesis of Novel Quinoline Derivatives.
  43. Lewis acid promoted aza Diels–Alder reactions of acyclic unactivated 5-dienyl pyrimidinones with N-arylimines: synthesis of novel quinoline derivatives
  44. SeO2‐Mediated Oxidation of 1,3‐Diazabuta‐1,3‐dienes: A Single‐Pot Synthesis of Functionalized 4‐Hydroxyimidazoles.
  45. SeO 2 -Mediated Oxidation of 1,3-Diazabuta-1,3-dienes: A Single-Pot Synthesis of Functionalized 4-Hydroxyimidazoles
  46. A Convenient Route to Biologically Important Quinazolines Using N‐Arylamino‐1,3‐diazabuta‐1,3‐dienes.
  47. Effect of the nature of substituents on aromatic aldehydes in microwave induced N-cyclohexylamidine–aldehyde condensation reactions
  48. Quinazolines Revisited: Search for Novel Anxiolytic and GABAergic Agents.
  49. A Catalyst‐ and Solvent‐Free Selective Approach to Biologically Important Quinazolines and Benzo[g]quinazoline.
  50. A catalyst- and solvent-free selective approach to biologically important quinazolines and benzo[g]quinazoline
  51. Quinazolines revisited: search for novel anxiolytic and GABAergic agents
  52. A Convenient Route to Biologically Important Quinazolines Using N -Arylamino-1,3-diazabuta-1,3-dienes
  53. Microwave Assisted Aza‐Wittig Reactions of N‐Imidoyliminophosphorane with Aldehydes: A Convenient and Selective Route to Quinazolines
  54. Microwave Assisted Aza‐Wittig Reactions of N‐Imidoyliminophosphorane with Aldehydes: A Convenient and Selective Route to Quinazolines.