All Stories

  1. Structural and adhesion properties of poly(ethyl 2-cyanoacrylate) post-cured at different temperatures and times
  2. An efficient catalytic method for the synthesis of pyrido[2,3-d ]pyrimidines as biologically drug candidates by using novel magnetic nanoparticles as a reusable catalyst
  3. ChemInform Abstract: Copper‐Free Oxime—Palladacycle‐Catalyzed Sonogashira Alkynylation of Deactivated Aryl Bromides and Chlorides in Water under Microwave Irradiation.
  4. ChemInform Abstract: Recent Advances in the Catalytic Enantioselective Reformatsky Reaction
  5. Microwave-assisted palladium-catalyzed highly regio- and stereoselective head to head dimerization of terminal aryl alkynes in water
  6. ChemInform Abstract: Palladium and Organocatalysis: an Excellent Recipe for Asymmetric Synthesis
  7. Enantioselective Conjugate Addition of Aldehydes and Ketones to Maleimides Catalyzed by a Chiral Bifunctional Nbenzoimidazol- cyclohexanediamine
  8. Improved procedure for the a-Arylation of chromanones by O-Protected ortho-Bromophenols
  9. Microwave Promoted Palladium-Catalyzed Oxyarylation of Dihydronaphthalene and Chromenes by o-Iodophenols and its Acetates
  10. Palladium and Organocatalysis: An Excellent Recipe for Asymmetric Synthesis
  11. Copper‐Free Oxime–Palladacycle‐Catalyzed Sonogashira Alkynylation of Deactivated Aryl Bromides and Chlorides in Water under Microwave Irradiation
  12. Recent Advances in the Catalytic Enantioselective Reformatsky Reaction
  13. ChemInform Abstract: Enantioselective Synthesis of Succinimides by Michael Addition of 1,3‐Dicarbonyl Compounds to Maleimides Catalyzed by a Chiral Bis(2‐aminobenzimidazole) Organocatalyst.
  14. ChemInform Abstract: Microwave‐Promoted Copper‐Free Sonogashira—Hagihara Couplings of Aryl Imidazolylsulfonates in Water.
  15. ChemInform Abstract: Microwave‐Promoted Suzuki—Miyaura Cross‐Coupling of Aryl Imidazolylsulfonates in Water.
  16. Microwave‐Promoted Copper‐Free Sonogashira–Hagihara Couplings of Aryl Imidazolylsulfonates in Water
  17. ChemInform Abstract: Oxime—Palladacycle‐Catalyzed Suzuki—Miyaura Arylation and Alkenylation of Aryl Imidazolesulfonates under Aqueous and Phosphane‐Free Conditions.
  18. Enantioselective Synthesis of Succinimides by Michael Addition of 1,3‐Dicarbonyl Compounds to Maleimides Catalyzed by a Chiral Bis(2‐aminobenzimidazole) Organocatalyst
  19. Microwave‐Promoted Suzuki–Miyaura Cross‐Coupling of Aryl Imidazolylsulfonates in Water
  20. ChemInform Abstract: Recyclable Silica‐Supported Prolinamide Organocatalysts for Direct Asymmetric Aldol Reaction in Water.
  21. Oxime–Palladacycle‐Catalyzed Suzuki–Miyaura Arylation and Alkenylation of Aryl Imidazolesulfonates under Aqueous and Phosphane‐Free Conditions
  22. ChemInform Abstract: Conjugate Addition of 1,3‐Dicarbonyl Compounds to Maleimides Using a Chiral C2‐Symmetric Bis(2‐aminobenzimidazole) as Recyclable Organocatalyst.
  23. ChemInform Abstract: Phosphane‐Free Suzuki—Miyaura Coupling of Aryl Imidazolesulfonates with Arylboronic Acids and Potassium Aryltrifluoroborates under Aqueous Conditions.
  24. Recyclable silica-supported prolinamide organocatalysts for direct asymmetric Aldol reaction in water
  25. ChemInform Abstract: Oxime Palladacycle‐Catalyzed Suzuki—Miyaura Alkenylation of Aryl, Heteroaryl, Benzyl, and Allyl Chlorides under Microwave Irradiation Conditions.
  26. Conjugate Addition of 1,3-Dicarbonyl Compounds to Maleimides Using a Chiral C2-Symmetric Bis(2-aminobenzimidazole) as Recyclable Organocatalyst
  27. ChemInform Abstract: Microwave‐Promoted Palladium‐Catalyzed Oxyarylation of Dihydronaphthalene and Chromenes by o‐Iodophenols and Its Acetates.
  28. Oxime Palladacycle‐Catalyzed Suzuki–Miyaura Alkenylation of Aryl, Heteroaryl, Benzyl, and Allyl Chlorides under Microwave Irradiation Conditions
  29. Microwave‐Promoted Palladium‐Catalysed Oxyarylation of Dihydronaphthalene and Chromenes by o‐Iodophenols and Its Acetates
  30. Organocatalyzed Conjugate Additions
  31. Prolinamide bridged silsesquioxane as an efficient, eco-compatible and recyclable chiral organocatalyst
  32. Phosphane-free Suzuki–Miyaura Coupling of Aryl Imidazolesulfonates with Arylboronic Acids and Potassium Aryltrifluoroborates under Aqueous Conditions
  33. ChemInform Abstract: Oxime‐Derived Palladacycles as Source of Palladium Nanoparticles
  34. ChemInform Abstract: Transition‐Metal‐Catalyzed Synthesis of Hydroxylated Arenes
  35. Transition‐Metal‐Catalyzed Synthesis of Hydroxylated Arenes
  36. Transition‐Metal‐Catalyzed Synthesis of Hydroxylated Arenes
  37. ChemInform Abstract: Efficient Suzuki—Miyaura Coupling of Deactivated Aryl Chlorides Catalyzed by an Oxime Palladacycle.
  38. Oxime-derived palladacycles as source of palladium nanoparticles
  39. ChemInform Abstract: Chiral 2‐Aminobenzimidazoles as Recoverable Organocatalysts for the Addition of 1,3‐Dicarbonyl Compounds to Nitroalkenes.
  40. ChemInform Abstract: Desulfonylation Reactions
  41. Efficient Suzuki-Miyaura Coupling of Deactivated Aryl Chlorides Catalyzed by an Oxime Palladacycle
  42. ChemInform Abstract: Water versus Solvent‐Free Conditions for the Enantioselective Inter‐ and Intramolecular Aldol Reaction Employing L‐Prolinamides and L‐Prolinethioamides as Organocatalysts.
  43. Chiral 2-Aminobenzimidazoles as Recoverable Organocatalysts for the Addition of 1,3-Dicarbonyl Compounds to Nitroalkenes†
  44. Water versus Solvent‐Free Conditions for the Enantioselective Inter‐ and Intramolecular Aldol Reaction Employing L‐Prolinamides and L‐Prolinethioamides as Organocatalysts
  45. Desulfonylation Reactions
  46. ChemInform Abstract: Prolinamides versus Prolinethioamides as Recyclable Catalysts in the Enantioselective Solvent‐Free Inter‐ and Intramolecular Aldol Reactions.
  47. ChemInform Abstract: Highly Efficient and Stereoselective Julia—Kocienski Protocol for the Synthesis of α‐Fluoro‐α,β‐unsaturated Esters and Weinreb Amides Employing 3,5‐Bis(trifluoromethyl)phenyl (BTFP) Sulfones.
  48. Prolinamides versus Prolinethioamides as Recyclable Catalysts in the Enantioselective Solvent‐Free Inter‐ and Intramolecular Aldol Reactions
  49. ChemInform Abstract: Towards Organocatalytic Polyketide Synthases with Diverse Electrophile Scope: Trifluoroethyl Thioesters as Nucleophiles in Organocatalytic Michael Reactions and Beyond.
  50. ChemInform Abstract: 3,5‐Bis(trifluoromethyl)phenyl Sulfones for the Highly Stereoselective Julia—Kocienski Synthesis of α,β‐Unsaturated Esters and Weinreb Amides.
  51. Application of Cyclopalladated Compounds as Catalysts for Heck and Sonogashira Reactions
  52. Highly Efficient and Stereoselective Julia–Kocienski Protocol for the Synthesis of α‐Fluoro‐α,β‐unsaturated Esters and Weinreb Amides Employing 3,5‐Bis(trifluoromethyl)phenyl (BTFP) Sulfones
  53. Towards Organocatalytic Polyketide Synthases with Diverse Electrophile Scope: Trifluoroethyl Thioesters as Nucleophiles in Organocatalytic Michael Reactions and Beyond
  54. 3,5‐Bis(trifluoromethyl)phenyl Sulfones for the Highly Stereoselective Julia–Kocienski Synthesis of α,β‐Unsaturated Esters and Weinreb Amides
  55. Towards Organocatalytic Polyketide Synthases with Diverse Electrophile Scope: Trifluoroethyl Thioesters as Nucleophiles in Organocatalytic Michael Reactions and Beyond
  56. Potassium Tetrachloropalladate(II)
  57. Asymmetric Conjugate Addition of Ketones to β‐Nitrostyrenes by Means of 1,2‐Amino‐Alcohol‐Derived Prolinamides as Bifunctional Catalysts.
  58. Organocatalytic Asymmetric Conjugate Additions
  59. Oxime Palladacycles Revisited: Stone‐Stable Complexes Nonetheless Very Active Catalysts
  60. Asymmetric Conjugate Addition of Ketones to β‐Nitrostyrenes by Means of 1,2‐Amino‐Alcohol‐Derived Prolinamides as Bifunctional Catalysts
  61. Organocatalytic asymmetric conjugate additions
  62. 3,5-Bis-(trifluoromethyl)phenyl sulfones in the synthesis of 3,5-disubstituted cyclopent-2-enones
  63. 3,5‐Bis(trifluoromethyl)phenyl Sulfones in the Julia—Kocienski Olefination — Application to the Synthesis of Tri‐ and Tetrasubstituted Olefins.
  64. Enantioselective Conjugate Addition of Ketones to β‐Nitrostyrenes Catalyzed by 1,2‐Amino Alcohol‐Derived Prolinamides.
  65. 3,5‐Bis(trifluoromethyl)phenyl Sulfones in the Julia–Kocienski Olefination – Application to the Synthesis of Tri‐ and Tetrasubstituted Olefins
  66. 3,5-Bis(trifluoromethyl)thiophenol
  67. Enantioselective conjugate addition of ketones to β-nitrostyrenes catalyzed by 1,2-amino alcohol-derived prolinamides
  68. Oxime palladacycles revisited: stone‐stable complexes nonetheless very active catalysts
  69. 3,5‐Bis(trifluoromethyl)phenyl Sulfones in the Direct Julia—Kocienski Olefination.
  70. 1,3,5-Trifluoro-2-nitrobenzene
  71. 3,5-Bis(trifluoromethyl)acetophenone
  72. Synthetic Applications of π‐Electron‐Deficient Sulfones
  73. 3,5-Bis(trifluoromethyl)phenyl Sulfones in the Direct Julia−Kocienski Olefination
  74. Synthetic Applications of π-Electron-Deficient Sulfones
  75. Synthesis of Ynones by Palladium‐Catalyzed Acylation of Terminal Alkynes with Acid Chlorides.
  76. 3,5‐Bis(trifluoromethyl)phenyl Sulfones in the Modified Julia Olefination: Application to the Synthesis of Resveratrol.
  77. Synthetic Applications of Oxime-Derived Palladacycles as Versatile Catalysts in Cross-Coupling Reactions
  78. 3,5-Bis(trifluoromethyl)phenyl sulfones in the modified Julia olefination: application to the synthesis of resveratrol
  79. C(sp2)‐C(sp) and C(sp)‐C(sp) Coupling Reactions Catalyzed by Oxime‐Derived Palladacycles.
  80. C(sp2)‐C(sp) and C(sp)‐C(sp) Coupling Reactions Catalyzed by Oxime‐Derived Palladacycles
  81. π‐Deficient 2‐(Arylsulfonyl)ethyl Esters as Protecting Groups for Carboxylic Acids.
  82. Synthesis and Reactivity of π‐Electron‐Deficient (Arylsulfonyl)acetates.
  83. A Copper‐ and Amine‐Free Sonogashira‐Type Coupling Procedure Catalyzed by Oxime Palladacycles.
  84. π-Deficient 2-(Arylsulfonyl)ethyl Esters as Protecting Groups for Carboxylic Acids
  85. Highly Active Oxime‐Derived Palladacycle Complexes for Suzuki—Miyaura and Ullmann‐Type Coupling Reactions.
  86. Synthesis and Reactivity of -Electron-Deficient (Arylsulfonyl)acetates
  87. A copper- and amine-free Sonogashira-type coupling procedure catalyzed by oxime palladacycles
  88. ChemInform Abstract: Oxime‐Derived Palladium Complexes as Very Efficient Catalysts for the Heck—Mizoroki Reaction.
  89. ChemInform Abstract: Simple, Economical and Environmentally Friendly Sulfone Synthesis.
  90. Highly Active Oxime-Derived Palladacycle Complexes for Suzuki−Miyaura and Ullmann-Type Coupling Reactions
  91. Simple, economical and environmentally friendly sulfone synthesis
  92. ChemInform Abstract: π‐Deficient α‐Arylsulfonyl Esters as Soft Nucleophiles in Organic Synthesis.
  93. Multigram scale synthesis of a useful aza-Diels–Alder adduct in a one-step procedure
  94. Oxime-Derived Palladium Complexes as Very Efficient Catalysts for the Heck–Mizoroki Reaction
  95. π-Deficient α-arylsulfonyl esters as soft nucleophiles in organic synthesis
  96. Remote Dipole Effects as a Means to Accelerate [Ru(amino alcohol)]-Catalyzed Transfer Hydrogenation of Ketones
  97. ChemInform Abstract: Oxime Palladacycles: Stable and Efficient Catalysts for Carbon—Carbon Coupling Reactions.
  98. ChemInform Abstract: 2‐Azanorbornyl Alcohols: Very Efficient Ligands for Ruthenium‐Catalyzed Asymmetric Transfer Hydrogenation of Aromatic Ketones.
  99. Oxime Palladacycles:  Stable and Efficient Catalysts for Carbon−Carbon Coupling Reactions
  100. 2-Azanorbornyl Alcohols:  Very Efficient Ligands for Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Aromatic Ketones
  101. ChemInform Abstract: Highly Diastereoselective Reaction of 2‐Azanorbornyl Enolates with Electrophiles
  102. Highly Diastereoselective Reaction of 2-Azanorbornyl Enolates with Electrophiles
  103. Ru(arene)(amino alcohol)-Catalyzed Transfer Hydrogenation of Ketones:  Mechanism and Origin of Enantioselectivity
  104. ChemInform Abstract: New Expedient Route to Both Enantiomers of Nonproteinogenic α‐Amino Acid Derivatives from the Unsaturated 2‐Aza‐bicyclo Moiety.
  105. ChemInform Abstract: Chiral N,N′‐ and N,O‐Bidentate Anionic Ligands. Preparation, Metal Complexation, and Evaluation in the Asymmetric Aziridination of Olefins.
  106. ChemInform Abstract: Deprotection of Sulfonyl Aziridines.
  107. New Expedient Route to Both Enantiomers of Nonproteinogenic α-Amino Acid Derivatives from the Unsaturated 2-Aza-Bicyclo Moiety
  108. Chiral N,N‘- and N,O-Bidentate Anionic Ligands. Preparation, Metal Complexation, and Evaluation in the Asymmetric Aziridination of Olefins
  109. Deprotection of Sulfonyl Aziridines
  110. Naphthalene-catalysed lithiation of N,N-diisopropylbenzamide and its methoxy derivatives
  111. (1S,3R,4R)-2-Azanorbornylmethanol, an Efficient Ligand for Ruthenium-Catalyzed Asymmetric Transfer Hydrogenation of Ketones
  112. Imidoyllithiums: Masked acyllithium reagents
  113. Readily available nitrene precursors increase the scope of Evans' asymmetric aziridination of olefins
  114. N-Boc-α-tosylsarcosine ethyl ester: An α-amido sulfone for the regio- and stereoselective synthesis of protected γ,δ-unsaturated N-methyl-α-amino acids by palladium-catalyzed nucleophilic substitution
  115. Preparation and evaluation of nitrene precursors (PhI=NSO2Ar) for the copper-catalyzed aziridination of olefins
  116. α-Nitrogenated Organolithium Compounds from N -(Tosylmethyl)amides
  117. α-Nitrogenated organolithium compounds from α-amidomethyl and α-aminomethyl sulfones
  118. Lithiated β-aminoalkyl sulfones as mono and dinucleophiles in the preparation of nitrogen heterocycles: Application to the synthesis of capsazepine
  119. Lithiated γ-Tosyl-Substituted Benzylmethallylamine:  New γ-Amino Methallyl Sulfone Anions in Organic Synthesis
  120. Lithiated γ-Tosyl-Substituted Benzylmethallylamine:  New γ-Amino Methallyl Sulfone Anions in Organic Synthesis
  121. Mono and dilithiation of benzyl[2-(tosylmethyl)-2-propenyl] amine: New γ-aminated allyl sulfone anions
  122. Tosylated lithium 2-(lithiomethyl)-2-propen-1-olate: a γ-alkoxide allyl sulfone anion in organic synthesis