All Stories

  1. Organocatalytic Reactions in Water
  2. Sulfamic Acid Catalyzed One‐Pot Three‐Component Synthesis of Spiro‐Oxindole Fused Dihydroquinazolinone Derivatives in Aqueous Medium
  3. Synthesis of Biologically Promising Spiroheterocycles through Electrolysis
  4. One-pot Three-component Synthesis of Fully and Diversely Functionalized Pyrans and Spiropyrans Using Sodium Formate as Catalyst in Aqueous Ethanol at Room Temperature
  5. Synthesis of Isatin-derived Heterocycles with Promising Anticancer Activities
  6. Camphorsulfonic Acid-Catalyzed Synthesis of a Series of 2-Aryl/heteroaryl/alkyl-1H-anthra[ 1,2-d]imidazole-6,11-dione Derivatives
  7. Synthesis of Structurally Diverse and Biologically Promising Polyheterocycles Involving Benzo[a]phenazin-5-ols
  8. Trisodium citrate dihydrate catalyzed one-pot four component synthesis of spiropyrano-indenoquinoxaline derivatives and their molecular docking analysis on the anti-cancer efficacies
  9. One‐Pot Three‐Component Synthesis of Biologically Promising Indenoquinoxaline Fused Spiroheterocycles Starting from 11H‐indeno[1,2‐b]quinoxalin‐11‐ones
  10. Ionic Liquid-promoted the Synthesis of Structurally Diverse Pyrans, Pyranannulated Heterocycles, and Spiropyrans
  11. Organocatalyzed multicomponent synthesis of densely functionalized bioactive pyridines
  12. 5 One-pot five/four-component synthesis of structurally diverse bioactive quinoxaline-annulated spiroheterocycles through the in situ formation of 11Hindeno[ 1,2-b]quinoxalin-11-ones
  13. 7 Solvent-free synthesis of structurally diverse bioactive xanthene derivatives under conventional heating conditions
  14. Sodium dodecyl sulfate catalyzed one-pot three-component synthesis of structurally diverse 2-amino-3-cyano-4-substitued-4H-chromenes in aqueous medium at room temperature
  15. Multicomponent Synthesis
  16. Solvent-Free Synthesis
  17. Non-Metal Catalyzed Synthesis
  18. Chapter 6. Ultrasound-assisted synthesis of bioactive 1,2,3-triazoles via click reactions
  19. Non-Conventional Synthesis
  20. Microwave-assisted Synthesis of Bioactive Heterocycles
  21. A Simple and Efficient Method for the Synthesis of Benzo[3,4-a]Phenazin-5-Ols and Benzo[f]Pyrido[b]Quinoxalin-5-ol Derivatives Using Trisodium Citrate as an Efficient Organo-Catalyst at Room Temperature
  22. Camphor sulfonic acid catalyzed one-pot pseudo three-component synthesis of a series of 1,8-dioxo-octahydroxanthenes and comparative crystal structures investigations and Hirshfeld surface analysis of five such derivatives
  23. Chapter 2. Organic transformations in nitromethane as solvent
  24. Ionic Liquids, Deep Eutectic Solvents, Crown Ethers, Fluorinated Solvents, Glycols and Glycerol
  25. Organic Synthesis, Natural Products Isolation, Drug Design, Industry and the Environment
  26. 9 Gadolinium triflate-catalyzed various organic transformations
  27. Rare Earth Elements
  28. Cyanuric chloride promoted various organic transformations
  29. Ultrasound-assisted Synthesis of Biologically Promising Organoselenium Scaffolds
  30. Sodium Dodecyl Sulphate Catalyzed One-Pot Three-Component Synthesis of Structurally Diverse 2-Amino-3-cyano Substituted Tetrahydrobenzo[b]pyrans and Spiropyrans in Water at Room Temperature
  31. Multicomponent synthesis of isatin-based bioactive heterocycles
  32. Glycine Catalyzed One-Pot Three-Component Synthesis of Structurally Diverse 2-Amino Substituted Pyran Annulated Heterocycles in Aqueous Ethanol under Refluxed Conditions
  33. Green Synthesis of Bioactive Heterocycles-Part 1A
  34. Mandelic acid catalyzed one-pot pseudo three-component synthesis of various trisubstituted methane derivatives at room temperature
  35. Role of the Heterocycles to Design Anti-Cancer Agents
  36. Carbon-Carbon and Carbon-Heteroatom
  37. Synthesis of Bioactive Scaffolds
  38. Trisodium citrate dihydrate catalyzed one-pot pseudo four-component synthesis of fully functionalized pyridine derivatives
  39. Synthesis, characterization and Hirshfeld surface analysis of 2-aminobenzothiazol with 4-fluorobenzoic acid co-crystal
  40. Glycine and its derivatives catalyzed one-pot multicomponent synthesis of bioactive heterocycles
  41. Preyssler catalyst: a heterogeneous polyacidic catalyst for the efficient synthesis of diverse bioactive heterocyclic scaffolds
  42. 3 Ultrasound-assisted heterogeneous catalysis in aqueous medium
  43. Heterocyclic Anticancer Agents
  44. Latest developments on the synthesis of bioactive organotellurium scaffolds
  45. Aqueous Mediated Heterogeneous Catalysis
  46. Chapter 11 Multicomponent synthesis of biologically promising pyrans and pyran annulated heterocycles using magnetically recoverable nanocatalysts
  47. Organocatalysis: a green tool for sustainable developments
  48. Industrial Applications
  49. Synthetic Applications
  50. A General Method for the Synthesis of 11H-Indeno[1,2-B]Quinoxalin- 11-Ones and 6H-Indeno[1,2-B]Pyrido[3,2-E]Pyrazin-6-One Derivatives Using Mandelic Acid as an Efficient Organo-catalyst at Room Temperature
  51. One-pot multi-component synthesis of diverse bioactive heterocyclic scaffolds involving 6-aminouracil or its N-methyl derivatives as a versatile reagent
  52. Naturally occurring, natural product inspired and synthetic heterocyclic anti-cancer drugs
  53. Lawsone (2-hydroxy-1,4-naphthaquinone) derived anticancer agents
  54. Naturally occurring bioactive biosurfactants
  55. Synthesis, X-ray crystal structure, Hirshfeld surface analysis, and molecular docking studies of DMSO/H2O solvate of 5-chlorospiro[indoline-3,7'-pyrano[3,2-c:5,6-c']dichromene]-2,6',8'-trione
  56. Microwave-Assisted Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions: Part 2B
  57. Supercritical Carbon Dioxide Mediated Organic Transformations
  58. Ultrasound-assisted synthesis of bioactive S-heterocycles
  59. Sulfonated β-cyclodextrins: efficient supramolecular organocatalysts for diverse organic transformations
  60. Baker’s yeast (Saccharomyces cerevisiae) catalyzed synthesis of bioactive heterocycles and some stereoselective reactions
  61. X-ray crystal structure analysis of 5-bromospiro[indoline-3,7'-pyrano[3,2-C:5,6-C']dichromene]-2,6',8'-trione
  62. A general method for the synthesis of structurally diverse quinoxalines and pyrido-pyrazine derivatives using camphor sulfonic acid as an efficient organo-catalyst at room temperature
  63. Organic Transformations by Following Green Credentials-Part 2
  64. p-Sulfonic Acid Calix[n]arene Catalyzed Synthesis of Bioactive Heterocycles: A Review
  65. Carbon-carbon and Carbon-heteroatom Bond Forming Reactions Under Greener Conditions - Part 2
  66. Organocatalyst: A Valuable Tool for the Carbon-carbon and Carbon-heteroatom bond Formations
  67. Camphor sulfonic acid catalyzed a simple, facile, and general method for the synthesis of 2-arylbenzothiazoles, 2-arylbenzimidazoles, and 3H-spiro[benzo[d]thiazole-2,3′-indolin]-2′-ones at room temperature
  68. Biosynthesis of bioactive zinc oxide nanoparticles
  69. Ionic liquid-mediated biocatalyzed organic transformations
  70. Microwave-assisted catalyst as well as solvent-free synthesis of bioactive heterocycles
  71. Tetrabutylammonium Bromide (TBAB) Catalyzed Synthesis of Bioactive Heterocycles
  72. Camphor sulfonic acid catalyzed facile and general method for the synthesis of 3,3'-(arylmethylene)bis(4-hydroxy-2H-chromen-2-ones), 3,3'-(arylmethylene)bis(2-hydroxynaphthalene-1,4-diones) and 3,3'-(2-oxoindoline-3,3-diyl)bis(2-hydroxynaphthalene-1,4-...
  73. Synthesis and Characterization of 2-Aminobenzothiazol and 1-Methylisatin Co-Сrystal
  74. Synthesis, Characterization, and Crystal Structure of 5'-Amino-4,4''-Dichloro-2'-Nitro-2',3'-Dihydro-[1,1':3',1''-Terphenyl]-4',4',6'(1'H)-Tricarbonitrile-Dimethyl Sulfoxide
  75. Microwave-assisted Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions - Part 1B
  76. Mandelic acid: An efficient organo-catalyst for the synthesis of 3-substituted- 3-hydroxy-indolin-2-ones and related derivatives in aqueous ethanol at room temperature
  77. Microwave-assisted Carbon-carbon and Carbon-heteroatom Bond Forming Reactions - Part 1A
  78. Recent Developments on the Synthesis of Biologically Significant bis/tris(indolyl)methanes under Various Reaction Conditions: A Review
  79. A General Method for the Synthesis of 3,3-bis(indol-3-yl)indolin-2-ones, bis(indol-3-yl)(aryl)methanes and tris(indol-3-yl)methanes Using Naturally Occurring Mandelic Acid as an Efficient Organo-catalyst in Aqueous Ethanol at Room Temperature
  80. Organic Transformations by Following Green Credentials- Part 1 (B)
  81. 9. Selenoamides, selenazadienes, and selenocarbonyls in organic synthesis
  82. Organoselenium Chemistry
  83. Carbon-Carbon and Carbon-Heteroatom Bond-forming Reactions under Greener Conditions-Part 1B
  84. Mandelic acid catalyzed one-pot three-component synthesis of α-aminonitriles and α-aminophosphonates under solvent-free conditions at room temperature
  85. Microwave assisted catalyst-free synthesis of bioactive heterocycles
  86. Catalytic Applications of Saccharin and its Derivatives in Organic Synthesis
  87. Carbon-Carbon and Carbon-Heteroatom Bond-forming Reactions under Greener Conditions-Part 1A
  88. Magnetically separable nanocatalyzed synthesis of bioactive heterocycles in water
  89. Water-Mediated Catalyst-Free Organic Transformations
  90. Recent advances in photo-irradiated synthesis of bioactive heterocycles
  91. Organic Transformations by Following Green Credentials- Part 1 (A)
  92. Naturally Occurring Organic Acid-catalyzed Facile Diastereoselective Synthesis of Biologically Active (E)-3-(arylimino)indolin-2-one Derivatives in Water at Room Temperature
  93. Multicomponent Synthesis of Biologically Relevant Spiroheterocycles in Water
  94. Ultrasound and Nano-Catalysts: An Ideal and Sustainable Combination to Carry out Diverse Organic Transformations
  95. Magnetically Separable Transition Metal Ferrites: Versatile Heterogeneous Nano-Catalysts for the Synthesis of Diverse Bioactive Heterocycles
  96. Camphorsulfonic Acid (CSA): An Efficient Organocatalyst for the Synthesis or Derivatization of Heterocycles with Biologically Promising Activities
  97. p ‐Dodecylbenzenesulfonic Acid: An Efficient Brønsted Acid‐Surfactant‐Combined Catalyst to Carry out Diverse Organic Transformations in Aqueous Medium
  98. One-Pot Pseudo Five Component Synthesis of Biologically Relevant 1,2,6-Triaryl-4-arylamino-piperidine-3-ene-3- carboxylates: A Decade Update
  99. Ultrasound and Ionic Liquid: An Ideal Combination for Organic Transformations
  100. Crystal Structure of Ethyl 6-Amino-5-cyano-4-(4-fluorophenyl)- 2,4-dihydropyrano[2,3-c]pyrazole-3-carboxylate
  101. 13. Ultrasound-assisted synthesis of organophosphorus compounds
  102. Recent Developments on Organo-bicyclo-bases Catalyzed Multicomponent Synthesis of Biologically Relevant Heterocycles
  103. [Bmim]PF6: An efficient tool for the synthesis of diverse bioactive heterocycles
  104. Recent developments on nano-ZnO catalyzed synthesis of bioactive heterocycles
  105. Synthesis, spectral characterization, and single crystal structure studies of biologically relevant bis-indoline heterocyclic scaffold
  106. [Bmim]BF4: A Versatile Ionic Liquid for the Synthesis of Diverse Bioactive Heterocycles
  107. Bismuth(III) triflate: An Efficient Catalyst for the Synthesis of Diverse Biologically Relevant Heterocycles
  108. Recent developments in the synthesis of biologically relevant selenium-containing scaffolds
  109. Recent developments on ultrasound-assisted one-pot multicomponent synthesis of biologically relevant heterocycles
  110. Recent developments on ultrasound assisted catalyst-free organic synthesis
  111. Recent Developments on Ultrasound-Assisted Synthesis of Bioactive N-Heterocycles at Ambient Temperature
  112. Recent developments on ultrasound-assisted organic synthesis in aqueous medium
  113. Sc(OTf)3 catalyzed carbon-carbon and carbon-heteroatom bond forming reactions: a review
  114. X-ray crystallography of methyl (6-amino-5-cyano-2-methyl-4-(2-nitrophenyl)-4H-pyran)-3-carboxylate
  115. Synthesis, spectroscopic characterization, and crystal structure of a novel indoline derivative
  116. Synthesis, spectroscopic characterization and crystallographic behavior of a biologically relevant novel indole-fused heterocyclic compound — Experimental and theoretical (DFT) studies
  117. ChemInform Abstract: Facile and Chemically Sustainable One-Pot Synthesis of a Wide Array of Fused O- and N-Heterocycles Catalyzed by Trisodium Citrate Dihydrate under Ambient Conditions.
  118. ChemInform Abstract: Sulfamic Acid-Catalyzed Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions: An Overview
  119. Sulfamic Acid-Catalyzed Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions: An Overview
  120. Room Temperature Metal-Free Synthesis of Aryl/Heteroaryl-Substituted Bis(6-aminouracil-5-yl)methanes Using Sulfamic Acid (NH2SO3H) as an Efficient and Eco-friendly Organo-Catalyst
  121. Synthesis, characterization, and crystal structure of 5,5″-Difluoro-1H,1″H-[3,3′:3′,3″-terindol]-2′(1′H)-one
  122. Facile and Chemically Sustainable One-Pot Synthesis of a Wide Array of FusedO- andN-Heterocycles Catalyzed by Trisodium Citrate Dihydrate under Ambient Conditions
  123. Crystal structure of 2-amino-7,7-dimethyl-5-oxo-4-(pyridin-4-yl)-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile hemihydrate
  124. Synthesis, characterization, and crystal structure of 2-amino-5-oxo-4-phenyl-4,5-dihydropyrano[3,2-c]chromene-3-carbonitrile
  125. Synthesis, characterization, and crystal structure of 2-amino-7-methyl-5-oxo-4-phenyl-4,5-dihydropyrano[3,2-c]pyran-3-carbonitrile
  126. X-ray studies of 2-amino-4-(3-nitrophenyl)-5-oxo-4,5-dihydropyrano[3,2-c] chromene-3-carbonitrile and 2-amino-7,7-dimethyl-4-(4-nitrophenyl)-5-oxo-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile
  127. X-ray studies of 2-amino-5-oxo-4-propyl-4,5-dihydropyrano[3,2-c]chromene-3-carbonitrile
  128. Catalyst-Free Organic Synthesis At Room Temperature in Aqueous and Non-Aqueous Media: An Emerging Field of Green Chemistry Practice and Sustainability
  129. ChemInform Abstract: Ammonium Chloride Catalyzed One-Pot Multicomponent Synthesis of 1,8-Dioxo-octahydroxanthenes and N-Aryl-1,8-dioxodecahydroacridines under Solvent Free Conditions.
  130. Ceric ammonium nitrate (CAN): an efficient and eco-friendly catalyst for the one-pot synthesis of alkyl/aryl/heteroaryl-substituted bis(6-aminouracil-5-yl)methanes at room temperature
  131. Ammonium chloride catalysed one-pot multicomponent synthesis of 1,8-dioxo-octahydroxanthenes and N-aryl-1,8-dioxodecahydroacridines under solvent free conditions
  132. Sunlight-induced rapid and efficient biogenic synthesis of silver nanoparticles using aqueous leaf extract of Ocimum sanctum Linn. with enhanced antibacterial activity
  133. Facile and One-Pot Access of 3,3-Bis(indol-3-yl)indolin-2-ones and 2,2-Bis(indol-3-yl)acenaphthylen-1(2 H )-one Derivatives via an Eco-Friendly Pseudo-Multicomponent Reaction at Room Temperature Using Sulfamic Acid as an Organo-Catalyst
  134. Crystal structure of 2-(4-nitrophenyl)-2-(phenylamino)propanenitrile and 2-(4-fluorophenylamino)-2-(4-nitrophenyl)propanenitrile
  135. Crystal structure of 5,5′-[(4-fluorophenyl)methylene]bis[6-amino-1,3-dimethylpyrimidine-2,4(1H,3H)-dione]
  136. 6-Amino-3-methyl-4-(3,4,5-trimethoxyphenyl)-2,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile
  137. Ethyl 6-amino-5-cyano-4-phenyl-2,4-dihydropyrano[2,3-c]pyrazole-3-carboxylate dimethyl sulfoxide monosolvate
  138. Eco-friendly, One-Pot Multicomponent Synthesis of Pyran Annulated Heterocyclic Scaffolds at Room Temperature Using Ammonium or Sodium Formate as Non-toxic Catalyst
  139. Facile and One-Pot Access to Diverse and Densely Functionalized 2-Amino-3-cyano-4H-pyrans and Pyran-Annulated Heterocyclic Scaffolds via an Eco-Friendly Multicomponent Reaction at Room Temperature Using Urea as a Novel Organo-Catalyst
  140. Facile synthesis of symmetrical bis(benzhydryl)ethers using p-toluenesulfonyl chloride under solvent-free conditions
  141. A Comparison Between Catalyst-Free and ZrOCl2⋅8H2O-Catalyzed Strecker Reactions for the Rapid and Solvent-Free One-Pot Synthesis of Racemic α-Aminonitrile Derivatives
  142. 2-Amino-7,7-dimethyl-5-oxo-4-(p-tolyl)-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile
  143. Trimethyl(triphenylmethoxy)silane