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  1. Organocatalytic enantioselective synthesis
  2. Chiral Squaramide-Catalyzed Enantioselective Decarboxylative Addition of β-Keto Acids to Isatin Imines
  3. ChemInform Abstract: α,α-Dicyanoolefins: Versatile Substrates in Organocatalytic Asymmetric Transformations
  4. ChemInform Abstract: Recent Advances in Iodine Monochloride Mediated Electrophilic Cyclizations
  5. Recent Advances in Iodine Monochloride Mediated Electrophilic Cyclizations
  6. ChemInform Abstract: Cinchona-Derived Thiourea Catalyzed Hydrophosphonylation of Ketimines - An Enantioselective Synthesis of α-Amino Phosphonates.
  7. Recent Developments on Thiourea Based Anticancer Chemotherapeutics
  8. Maleimide as an efficient nucleophilic partner in the aza-Morita–Baylis–Hillman reaction: synthesis of chiral 3-substituted-3-aminooxindoles
  9. Stereoselective synthesis of 3-amino-2-oxindoles from isatin imines: new scaffolds for bioactivity evaluation
  10. ChemInform Abstract: Organocatalytic Enantioselective aza-Henry Reaction of Ketimines Derived from Isatins: Access to Optically Active 3-Amino-2-oxindoles.
  11. Pseudomonas gessardii growing cells as a new biocatalyst for asymmetric synthesis of α-bromohydrins
  12. ChemInform Abstract: Design of Peptidyl Thiourea Derivatives as Organocatalysts for the Asymmetric Ring Opening of meso-Stilbene Oxides.
  13. Cinchona-derived thiourea catalyzed hydrophosphonylation of ketimines—an enantioselective synthesis of α-amino phosphonates
  14. ChemInform Abstract: Organocatalytic Asymmetric Friedel-Crafts Reaction of 1-Naphthols with Isatins: An Enantioselective Synthesis of 3-Aryl-3-hydroxy-2-oxindoles.
  15. Synthesis and Stereochemistry-Activity Relationship of Chiral Thiourea Derivatives as Potential Anticancer Agents
  16. Inside Cover: Design of Peptidyl Thiourea Derivatives as Organocatalysts for the Asymmetric Ring Opening of meso‐Stilbene Oxides (Asian J. Org. Chem. 6/2014)
  17. Design of Peptidyl Thiourea Derivatives as Organocatalysts for the Asymmetric Ring Opening of meso‐Stilbene Oxides
  18. Primary-tertiary diamine-catalyzed Michael addition of ketones to isatylidenemalononitrile derivatives
  19. Organocatalytic Asymmetric Friedel–Crafts Reaction of Sesamol with Isatins: Access to Biologically Relevant 3‐Aryl‐3‐hydroxy‐2‐oxindoles
  20. Organocatalytic asymmetric Friedel–Crafts reaction of 1-naphthols with isatins: an enantioselective synthesis of 3-aryl-3-hydroxy-2-oxindoles
  21. ChemInform Abstract: Pyrrolidine Catalyzed Diastereoselective Direct Aldol Reaction in Water: A Green Approach.
  22. Organocatalytic enantioselective aza-Henry reaction of ketimines derived from isatins: access to optically active 3-amino-2-oxindoles
  23. Cinchonidine thiourea catalyzed asymmetric addition of phenols to oxindole derivatives
  24. ChemInform Abstract: Organocatalytic Asymmetric Direct Aldol Reaction of Pyruvic Aldehyde Dimethyl Acetal with Isatin Derivatives.
  25. ChemInform Abstract: Organocatalytic Enantioselective Aza‐Friedel—Crafts Reaction of Sesamols with N‐Sulfonylimines Catalyzed by 6′‐OH Cinchona Alkaloids.
  26. Highly enantioselective kinetic resolution of trans-2-(phenylthio)cyclohexanol derivatives by immobilized Candida antartica B lipase
  27. ChemInform Abstract: Organocatalyzed Direct Asymmetric Aldol Reaction of Isatins in Water: Low Catalyst Loading in Command.
  28. Organocatalytic enantioselective aza-Friedel–Crafts reaction of sesamols with N-sulfonylimines catalyzed by 6′-OH Cinchona alkaloids
  29. ChemInform Abstract: Organocatalytic Asymmetric Synthesis of 3‐Amino‐2‐oxindole Derivatives Bearing a Tetra‐Substituted Stereocenter
  30. ChemInform Abstract: Mechanochemistry‐Assisted Asymmetric Organocatalysis: A Sustainable Approach
  31. Inside Cover: Organocatalytic Enantioselective Morita–Baylis–Hillman Reaction of Maleimides with Isatins (Asian J. Org. Chem. 7/2013)
  32. Organocatalytic Asymmetric Direct Aldol Reaction of Pyruvic Aldehyde Dimethyl Acetal with Isatin Derivatives
  33. Organocatalytic Enantioselective Morita–Baylis–Hillman Reaction of Maleimides with Isatins
  34. Organocatalyzed direct asymmetric aldol reaction of isatins in water: low catalyst loading in command
  35. ChemInform Abstract: D‐Camphor‐10‐sulfonic Acid: A Water Compatible Organocatalyst for Friedel—Crafts Reaction of Indoles with Electron Deficient Olefins.
  36. ChemInform Abstract: Asymmetric Organocatalytic Addition Reactions of Maleimides: A Promising Approach Towards the Synthesis of Chiral Succinimide Derivatives
  37. Organocatalytic asymmetric synthesis of 3-amino-2-oxindole derivatives bearing a tetra-substituted stereocenter
  38. ChemInform Abstract: Chiral Amine Catalyzed Enantio‐ and Diastereoselective Michael Reaction in Brine.
  39. ChemInform Abstract: Catalytic Asymmetric Synthesis of 3‐Hydroxyoxindole, a Potentially Bioactive Molecule
  40. Mechanochemistry assisted asymmetric organocatalysis: A sustainable approach
  41. Asymmetric Organocatalytic Addition Reactions of Maleimides: A Promising Approach Towards the Synthesis of Chiral Succinimide Derivatives
  42. ChemInform Abstract: Recent Advances in Asymmetric Organocatalytic Conjugate Addition of Arenes and Hetero‐arenes
  43. Grinding‐Assisted Asymmetric Organocatalysis: A Solvent‐free Approach to the Formation of Vicinal Quaternary and Tertiary Stereocenters
  44. Chiral amine catalyzed enantio- and diastereoselective Michael reaction in brine
  45. ChemInform Abstract: Aromatic Hydroxyl Group — A Hydrogen Bonding Activator in Bifunctional Asymmetric Organocatalysis.
  46. ChemInform Abstract: Facile Construction of Vicinal Quaternary and Tertiary Stereocenters via Regio‐ and Stereoselective Organocatalytic Michael Addition to Nitrodienes.
  47. Aromatic hydroxyl group—a hydrogen bonding activator in bifunctional asymmetric organocatalysis
  48. Catalytic asymmetric synthesis of 3-hydroxyoxindole: a potentially bioactive molecule
  49. Recent advances in asymmetric organocatalytic conjugate addition of arenes and hetero-arenes
  50. Bioresolution of benzyl glycidyl ether using whole cells of Bacillus alcalophilus
  51. Facile Construction of Vicinal Quaternary and Tertiary Stereocenters via Regio‐ and Stereoselective Organocatalytic Michael Addition to Nitrodienes
  52. ChemInform Abstract: Asymmetric syn‐Selective Direct Aldol Reaction of Protected Hydroxyacetone Catalyzed by Primary Amino Acid Derived Bifunctional Organocatalyst in the Presence of Water.
  53. ChemInform Abstract: Catalyst‐Free and Solventless Hantzsch Ester Mediated Reduction of Nitroolefins at Elevated Temperature.
  54. ChemInform Abstract: Asymmetric Organocatalytic Aza‐Friedel—Crafts Reaction of Naphthols with N‐Sulfonyl Imines.
  55. ChemInform Abstract: Recent Developments in the Asymmetric Hydrolytic Ring Opening of Epoxides Catalyzed by Microbial Epoxide Hydrolase.
  56. Asymmetric Organocatalytic Aza‐Friedel–Crafts Reaction of Naphthols with N‐Sulfonyl Imines
  57. Asymmetric syn-selective direct aldol reaction of protected hydroxyacetone catalyzed by primary amino acid derived bifunctional organocatalyst in the presence of water
  58. Recent developments in the asymmetric hydrolytic ring opening of epoxides catalysed by microbial epoxide hydrolase
  59. ChemInform Abstract: Asymmetric Addition of Indoles to Isatins Catalyzed by Bifunctional Modified Cinchona Alkaloid Catalysts.
  60. ChemInform Abstract: Novel Bisstyryl Derivatives of Bakuchiol: Targeting Oral Cavity Pathogens.
  61. ChemInform Abstract: Thiourea Catalyzed Aminolysis of Epoxides under Solvent‐Free Conditions. Electronic Control of Regioselective Ring Opening.
  62. Asymmetric Addition of Indoles to Isatins Catalysed by Bifunctional Modified Cinchona Alkaloid Catalysts
  63. Novel bisstyryl derivatives of bakuchiol: Targeting oral cavity pathogens
  64. ChemInform Abstract: A Highly Diastereoselective Synthesis of Homoallylic Alcohol/Amine Appended Uracils: The Role of the Uracil C-4 Carbonyl in Diastereoselectivity Control.
  65. Bacillus alcalophilus MTCC10234 catalyzed enantioselective kinetic resolution of aryl glycidyl ethers
  66. Thiourea catalyzed aminolysis of epoxides under solvent free conditions. Electronic control of regioselective ring opening
  67. ChemInform Abstract: Allyl Tetrahydropyranyl Ether: A Versatile Alcohol/Thiol Protecting Reagent.
  68. Allyl tetrahydropyranyl ether: a versatile alcohol/thiol protecting reagent
  69. The pH of the reaction controls the stereoselectivity of organocatalyzed direct aldol reactions in water
  70. ChemInform Abstract: Protonated (S)‐Prolinamide Derivatives—Water Compatible Organocatalysts for Direct Asymmetric Aldol Reaction.
  71. Protonated (S)-prolinamide derivatives—water compatible organocatalysts for direct asymmetric aldol reaction
  72. An expedient chemo-enzymatic method for the synthesis of optically active masked 1,2-amino alcohols
  73. Short‐chain ester synthesis by transesterification employing poly (MAc‐co‐DMA‐cl‐MBAm) hydrogel‐bound lipase of Bacillus coagulans MTCC‐6375
  74. Pyrrolidine‐Catalyzed Regioselective and Diastereoselective Direct Aldol Reaction in Water.
  75. The Formation of Novel 1,3‐Dioxolanes: Atypical Baylis—Hillman Reaction of a Sesquiterpene Lactone Parthenin.
  76. Synthesis of ethyl propionate catalyzed by poly(N‐AEAAm‐co‐AAc)‐cl‐MBAm hydrogel‐immobilized lipase ofBacillus coagulansMTCC‐6375
  77. Enantiocomplementary reduction of 3-phenylthiopropan-2-one by Bacillus sp.: Effect of medium components
  78. The formation of novel 1,3-dioxolanes: atypical Baylis–Hillman reaction of a sesquiterpene lactone parthenin
  79. Properties of poly(AAc‐co‐HPMA‐cl‐EGDMA) hydrogel‐bound lipase ofPseudomonas aeruginosaMTCC‐4713 and its use in synthesis of methyl acrylate
  80. Small Organic Molecule Catalyzed Enantioselective Direct Aldol Reaction in Water.
  81. Odoriferous Cyclic Ethers via Co‐Halogenation Reaction: Facile Preparation of Nerol Oxide, Florol®, Florol® Methyl Ether, and Pityol® Methyl Ether
  82. Small organic molecule catalyzed enantioselective direct aldol reaction in water
  83. Biodegradation of azo dye C.I. Acid Red 88 by an anoxic–aerobic sequential bioreactor
  84. Enhancement of Ethyl Propionate Synthesis by poly (AAc-co-HPMA-cl-MBAm)-immobilized  Pseudomonas aeruginosa MTCC-4713, Exposed to Hg2+and NH4+Ions
  85. Purification and properties of a novel extra-cellular thermotolerant metallolipase of Bacillus coagulans MTCC-6375 isolate
  86. Characteristics of poly(AAc5‐co‐HPMA3‐cl‐EGDMA15) hydrogel‐immobilized lipase of Pseudomonas aeruginosa MTCC‐4713
  87. Catalytic potential of a poly(AAc‐co‐HPMA‐cl MBAm)‐matrix‐immobilized lipase from a thermotolerant Pseudomonas aeruginosa MTCC‐4713
  88. Purification of a Moderate ThermotolerantBacillus coagulansBTS1 Lipase and its Properties in a Hydro-gel System
  89. Methacrylic acid and dodecyl methacrylate (MAc‐DMA) hydrogel for enhanced catalytic activity of lipase of Bacillus coagulans MTCC‐6375
  90. Comparative studies on potential of consortium and constituent pure bacterial isolates to decolorize azo dyes
  91. Effect of Solvents and Kinetic Parameters on Synthesis of Ethyl Propionate Catalysed by Poly (AAc-co-HPMA-cl-MBAm)-Matrix-Immobilized Lipase of Pseudomonas aeruginosa BTS-2.
  92. Decolorization of various azo dyes by bacterial consortium
  93. Electron Deficiency of Aldehydes Controls the Pyrrolidine Catalyzed Direct Cross‐Aldol Reaction of Aromatic/Heterocyclic Aldehydes and Ketones in Water.
  94. Protonated chiral prolinamide catalyzed enantioselective direct aldol reaction in water
  95. Electron deficiency of aldehydes controls the pyrrolidine catalyzed direct cross-aldol reaction of aromatic/heterocyclic aldehydes and ketones in water
  96. Synthesis of β-adrenergic blockers (R)-(−)-nifenalol and (S)-(+)-sotalol via a highly efficient resolution of a bromohydrin precursor
  97. A Simple One‐Step Protocol for the Olefination of Vinylogous Formamides.
  98. Biotreatment of Simulated Textile Dye Effluent Containing Malachite Green by an Up-Flow Immobilized Cell Bioreactor
  99. Properties of an immobilized lipase ofBacillus coagulansBTS-1
  100. Biological treatment of textile dye Acid violet-17 by bacterial consortium in an up-flow immobilized cell bioreactor
  101. A simple one-step protocol for the olefination of vinylogous formamides
  102. Biodegradation of acid blue-15, a textile dye, by an up-flow immobilized cell bioreactor
  103. Isolation and characterization of microorganisms capable of decolorizing various triphenylmethane dyes
  104. Kinetic resolution of 1-chloro-3-(1-naphthyloxy)-2-propanol, an intermediate in the synthesis of β-adrenergic receptor blockers
  105. Novel Indium‐Mediated Ternary Reactions Between Indole‐3‐carboxaldehydes—Allyl Bromide—Enamines: Facile Synthesis of Bisindolyl‐ and Indolyl‐Heterocyclic Alkanes.
  106. Chemoenzymatic Synthesis of Optically Active Heterocyclic Homoallylic and Homopropargylic Alcohols.
  107. Novel indium-mediated ternary reactions between indole-3-carboxaldehydes–allyl bromide–enamines: facile synthesis of bisindolyl- and indolyl-heterocyclic alkanes
  108. Novel Indium‐Mediated Deoxygenative α,α‐Diallylation of Indole‐ and Pyrrole‐3‐carboxaldehydes.
  109. Chemoenzymatic synthesis of optically active heterocyclic homoallylic and homopropargylic alcohols
  110. First Chemoenzymatic Synthesis of Optically Active Uracil and Chromen‐4‐one Substituted Homoallylic Alcohols: An Entry into Chiral Pool.
  111. Novel indium-mediated deoxygenative α,α-diallylation of indole- and pyrrole-3-carboxaldehydes
  112. Kinetic Resolution of Heteroaryl β‐Hydroxy Sulfides Catalyzed by Humicola lanuginosa Lipase.
  113. ChemInform Abstract: The Efficient Allylations of 2‐Oxocarboxylic Acids. Synthesis of 2‐Allyl Derivatives of 2‐Hydroxycarboxylic Acids.
  114. Synthesis of enantioselecvtive beta- and gamma- hydroxy sulfides have been achieved.
  115. ChemInform Abstract: Humicola lanuginosa Lipase Catalyzed Enantioselective Resolution of β‐Hydroxy Sulfides: Versatile Synthons for Enantiopure β‐Hydroxy Sulfoxides.
  116. Kinetic resolution of heteroaryl β-hydroxy sulfides catalyzed by Humicola lanuginosa lipase
  117. ChemInform Abstract: Diastereoselective Synthesis of 1‐Allyl and 1,2‐Bis(allyl)‐1,2‐diols: Versatile Synthons for Substituted Tetrahydrofuran Derivatives.
  118. First Chemoenzymatic Synthesis of Optically Active Uracil and Chromen-4-one Substituted Homoallylic Alcohols: An Entry into Chiral Pool
  119. The Efficient Allylations of 2-Oxocarboxylic Acids. Synthesis of 2-Allyl Derivatives of 2-Hydroxycarboxylic Acids
  120. Humicola lanuginosa lipase-catalyzed enantioselective resolution of β-hydroxy sulfides: versatile synthons for enantiopure β-hydroxy sulfoxides
  121. A highly diastereoselective synthesis of homoallylic alcohol/amine appended uracils: the role of the uracil C-4 carbonyl in diastereoselectivity control
  122. Diastereoselective Synthesis of 1-Allyl and 1,2-bis(Allyl)-1,2-diols: Versatile Synthons For Substituted Tetrahydrofuran Derivatives
  123. ChemInform Abstract: Indium‐Mediated Barbier Allylations of Hydroxyanthraquinones: An Expedient Synthesis of Novel 10‐Alkenyl‐10‐hydroxy‐9(10H)‐anthracenones.
  124. Indium-Mediated Barbier allylations of Hydroxyanthraquinones: An Expedient synthesis of Novel 10-Alkenyl-10-Hydroxy-9(10H)-Anthracenones
  125. ChemInform Abstract: Enamine‐Induced Ring Transformations of 6‐Substituted 5‐Formyl‐1,3‐dimethyluracils.
  126. ChemInform Abstract: Acid‐Catalyzed Reactions of 5‐Formyluracils with Enamines. A Facile Synthesis of 5‐Acylvinyluracils.
  127. Acid catalysed reactions of 5-formyluracils with enamines. A facile synthesis of 5-acylvinyluracils
  128. Enamine-induced Ring Transformations of 6-Substituted 5-Formyl-1,3-dimethyluracils†
  129. Facile Synthesis of 5-(Substituted vinyl)-uracil Derivatives through Knoevenagel and Stobbe type Condensations of 5-Formyluracils
  130. ChemInform Abstract: A Facile Single Pot Synthesis of 5‐Vinyl‐1,3‐dimethyluracil from 5‐ Formyl‐1,3‐dimethyluracil.
  131. ChemInform Abstract: Variable Reactivity Pattern of 6‐Cyano‐1,3‐dimethyluracil in PTC Reactions with Carbanions.
  132. ChemInform Abstract: Acid‐Catalyzed Enamine‐Induced Transformations of 1,3‐Dimethyl‐5‐ formyluracil. A Unique Annulation Reaction with Enaminones.
  133. ChemInform Abstract: Heterocyclic Transformations. Part 7. Unprecedented Transformations of 1,3‐Dialkyl‐5‐formyluracils to 1,3‐Dialkyl‐7‐hydroxyquinazolines.
  134. ChemInform Abstract: Heterocyclic Transformations. Part 6. Studies on the Reactions of 3‐ Benzyl‐6‐methyl‐1,3‐oxazine‐2,4(3H)‐dione with α‐Amino and Hydroxy Amides.
  135. Acid catalysed enamine induced transformations of 1,3-dimethyl-5-formyluracil. A unique annulation reaction with enaminones
  136. Reactions of diazines with nucleophiles—IV1. the reactivity of 5-bromo-1,3,6-trimethyluracil with thiolate ions—substitution versus X-philic versus single electron transfer reactions
  137. Heterocyclic transformations. Part 7. Unprecedented transformations of 1,3-dialkyl-5-formyluracils to 1,3-dialkyl-7-hydroxyquinazolines
  138. ChemInform Abstract: A Facile Reduction of Uracil Derivatives by 1,3‐Propanedithiol.
  139. ChemInform Abstract: Phase‐Transfer Catalyzed Oxidative Arylthiolation of 1,3,6‐ Trimethyluracil and Its 5‐Bromo Derivatives.
  140. ChemInform Abstract: Reactions of Diazines with Nucleophiles. Part 3. Umpolung of Reactivity at the C‐5 Position of Uracil. Facile Nucleophilic Reactions of Thiolate Ions at C‐5 of 6‐Cyano‐1,3‐dimethyluracil to Procure 5‐Alkyl‐ or 5‐Aryl‐thio‐1,3‐dimet...
  141. ChemInform Abstract: Phase‐Transfer‐Catalyzed Reactions of Thiolate Ions with 5‐Bromo‐1,3‐ dimethyluracil. A Reinvestigation of the Mechanism.
  142. Phase Transfer Catalysed Oxidative Arylthiolation of 1,3,6-Trimethyluracil and Its 5-Bromo Derivative
  143. Umpolung of reactivity at the C-5 position of uracil: 1,2 facile nucleophilic reactions of thiolate ions at C-5 of 6-cyano-1,3-dimethyluracil to procure 5-alkyl or 5-aryl-thio-1,3-dimethyluracils
  144. Heterocyclic transformations. Part 3. Thiolate ion-induced transformations of 6-methyl-1,3-oxazine-2,4(3H)-diones to 3-(alkyl/arylthio)but-2-enamides
  145. 'Umpolung' of Reactivity at C-5 Position of Uracil: An Unprecedented Nucleophilic Reaction of Thiolane Ion at C-5 of 6-Cyano-1,3-dimethyluracil