All Stories

  1. Distibine versus Diphosphine Ligands: Modulating the Properties of Isostructural Au 13 Cu 2 Nanoclusters
  2. Lewis Acid‐Promoted Domino Processes for the Synthesis of Homoallylic Amines, Quinolines and Tetrahydroquinolines
  3. Hydrogen bonding network-enabled Brønsted acid-catalyzed Friedel–Crafts reactions: a green approach to access unsymmetrical diaryl- and triarylmethanes
  4. Lewis Acid-Promoted Typical Friedel–Crafts Reactions Using DMSO as a Carbon Source
  5. Brønsted Acid Mediated Brønsted Acid-Catalyzed Friedel-Crafts Reactions of Aldehydes and Ketones with Arenes: A Mild Protocol for the Synthesis of Symmetrical/Unsymmetrical Di/Trisubstitutedmethanes.
  6. Development of Transition‐Metal‐Free Lewis Acid‐Initiated Double Arylation of Aldehyde: A Facile Approach Towards the Total Synthesis of Anti‐Breast‐Cancer Agent
  7. An Introduction on Evolution of Azole Derivatives in Medicinal Chemistry
  8. An Overview on Biological Activities of 1,2,3-Triazole Derivatives
  9. An Overview on Biological Activities of Oxazole, Isoxazoles and 1,2,4-Oxadiazoles Derivatives
  10. An Overview on Biological Activity of Benzimidazole Derivatives
  11. An Overview on Biological Evaluation of Tetrazole Derivatives
  12. Overview on Biological Activities of Imidazole Derivatives
  13. Overview on Biological Activities of Pyrazole Derivatives
  14. Overview on Biological Activities of Thiazole Derivatives
  15. Organocatalytic Decarboxylation and Dual C(sp3)−H Bond Functionalization Toward Facile Access to Divergent 2,6‐Diarylpyridines
  16. Transition-Metal-Free Transfer Hydrogenative Cascade Reaction of Nitroarenes with Amines/Alcohols: Redox-Economical Access to Benzimidazoles
  17. Csp–Cspbond cleavage and fragment coupling: a transition metal-free “extrusion and recombination” approach towards synthesis of 1,2-diketones
  18. HFIP-mediated strategy towards β-oxo amides and subsequent Friedel-Craft type cyclization to 2‑quinolinones using recyclable catalyst
  19. A Facile C‐H Insertion Strategy using Combination of HFIP and Isocyanides: Metal‐Free Access to Azole Derivatives
  20. Comprehensive Strategies for the Synthesis of Isoquinolines: Progress Since 2008
  21. Copper‐Catalyzed [2+2+1+1] Annulation for the Regioselective Synthesis of 2,6‐Diarylpyridines via C1‐Insertion and Subsequent Cyclization
  22. Recent Advances in Pyridine‐Based Organocatalysis and its Application towards Valuable Chemical Transformations
  23. Transition-metal-free variant of Glaser- and Cadiot-Chodkiewicz-type Coupling: Benign access to diverse 1,3-diynes and related molecules
  24. Conversion of alkynes into 1,2-diketones using HFIP as sacrificial hydrogen donor and DMSO as dihydroxylating agent
  25. Amino‐Acid‐Mediated Aerobic Oxidation of Organoborons for the Synthesis of Phenolic Derivatives Using Single Electron Transfer
  26. Niacin as a Potent Organocatalyst towards the Synthesis of Quinazolines Using Nitriles as C–N Source
  27. Decarboxylative cyclization of amino acids towards the Regioselective synthesis of 2,4-diarylpyridines via relay Fe(III)/In(III)-catalysis
  28. An organocatalytic C–C bond cleavage approach: a metal-free and peroxide-free facile method for the synthesis of amide derivatives
  29. Reagent-Controlled Divergent Synthesis of 2-Amino-1,3-Benzoxazines and 2-Amino-1,3-Benzothiazines
  30. Mo(VI)-catalyzed Synthesis of 2-Aryl-2H-indazoles Using Pinacol Mediated Deoxygenation of Nitroaromatics
  31. Gold‐Catalyzed Facile Protocol towards the Efficient Access of Azetidinyl Esters, β‐Amino Esters and δ‐Amino Esters using Simple Substrates
  32. Pd-Catalyzed Decarboxylation and Dual C(sp3)–H Functionalization Protocols for the Synthesis of 2,4-Diarylpyridines
  33. Organocatalytic oxidative synthesis of C2-functionalized benzoxazoles, naphthoxazoles, benzothiazoles and benzimidazoles
  34. Copper-Catalyzed Site-Selective Oxidative C−C Bond Cleavage of Simple Ketones for the Synthesis of Anilides and Paracetamol
  35. Divergent Synthesis of Quinazolines Using Organocatalytic Domino Strategies under Aerobic Conditions
  36. Facile Protocols towards C2-Arylated Benzoxazoles using Fe(III)-Catalyzed C(sp 2-H) Functionalization and Metal-Free Domino Approach
  37. Efficient Syntheses of Diverse N-Heterocycles: The Molybdenum(VI)-Catalyzed Reductive Cyclization of Nitroarenes using Pinacol as a Deoxygenating­ Agent
  38. The facile and efficient organocatalytic platform for accessing 1,2,4-selenadiazoles and thiadiazoles under aerobic conditions
  39. Pd-catalyzed domino reactions of nitroaromatics: A surrogate access towards the saturated N -heterocycles
  40. Novel Domino Routes for the Synthesis of N-Heterocycles via Reductive Cyclization of β-(N-2-Nitroaryl)-α,β-unsaturated Ketones