All Stories

  1. Photocatalytic CO2 Reduction Using an Iron–Bipyridyl Complex Supported by Two Phosphines for Improving Catalyst Durability
  2. Selective Reduction of Carboxylic Acids to Alcohols in the Presence of Alcohols by a Dual Bulky Transition-Metal Complex/Lewis Acid Catalyst
  3. Bulkiness of catalyst for photocatalytic CO2 reduction
  4. Phosphorus-Based Organocatalysis for the Dehydrative Cyclization of N-(2-Hydroxyethyl)amides into 2-Oxazolines
  5. ruthenium catalyst for CO2 photo-reduction
  6. CO2 as C1 source for photocatalytic C–C bond formation
  7. Development of Effective Bidentate Diphosphine Ligands of Ruthenium Catalysts toward Practical Hydrogenation of Carboxylic Acids
  8. C(sp3)–H bond functionalization with styrenes via hydrogen-atom transfer to an aqueous hydroxyl radical under photocatalysis
  9. Preparation of a platinum nanoparticle catalyst located near photocatalyst titanium oxide and its catalytic activity to convert benzyl alcohols to the corresponding ethers
  10. Catalyzing a Zero-Carbon World by Harvesting Energy from Living Cells
  11. catechol-coordinated P(V) for dehydrate amide bond formation
  12. A single, mononuclear Ir complex for CO2 photoreduction
  13. natural amino acids goes to beta-amino alcohols
  14. Amine gives secondary amine and NH3
  15. So many drugs have N-methyl and N-ethyl units. Using alcohols, how we could synthesize drugs?
  16. One boron or two-connected borons, which would be better for amide bond formation?
  17. Interplay of Cu and Au, immobilized on TiO2 (P25) for N-alkylation under light!
  18. carboxylic acids (CAs) and their reduced form alcohols are renewables, going to SDGs!!
  19. Light energy for synthesizing propylene and fragrance lavandulol from renewable resources
  20. Trimethylaluminum
  21. High valent metal complex turns catalysis on its head for a sustainable future
  22. Ruthenium catalyst breaks down plastic wastes by hydrogenation
  23. Dehydrogenation of Primary Aliphatic Alcohols by Au/TiO2 Photocatalysts
  24. Synthesis of morphan derivatives with additional substituents in 8-position
  25. (PN)2Ru complexes for hydrogen attachment and detachment
  26. Investigation of the Corey Bromolactamization withN-Functionalized Allylamines
  27. Milestone discovery: molecular catalyst design for hydrogenation of carboxylic acids (CAs)
  28. N-Methylation of Amines with Methanol at Room Temperature
  29. Stereoselective Synthesis ofcis,cis-Configured Perhydroquinoxaline-5-Carbonitrile from Cyclohex-2-en-1-ol
  30. ChemInform Abstract: Catalytic Fluoride Triggers Dehydrative Oxazolidinone Synthesis from CO2.
  31. ChemInform Abstract: Stereoselective Synthesis of cis,cis-Configured Vicinal Triamines.
  32. One-step synthesis of patterned polymer brushes by photocatalytic microcontact printing
  33. Hydration of nitriles to amides by a chitin-supported ruthenium catalyst
  34. Catalytic fluoride triggers dehydrative oxazolidinone synthesis from CO2
  35. Stereoselective Synthesis ofcis,cis-Configured Vicinal Triamines
  36. Bromolactamization: Key Step in the Stereoselective Synthesis of Enantiomerically Pure, cis -Configured Perhydropyrroloquinoxalines
  37. Synthesis of propylene from renewable allyl alcohol by photocatalytic transfer hydrogenolysis
  38. ChemInform Abstract: Dehydrative Synthesis of Chiral Oxazolidinones Catalyzed by Alkali Metal Carbonates under Low Pressure of CO2.
  39. ChemInform Abstract: Catalytic Hydrogenation of Unactivated Amides Enabled by Hydrogenation of Catalyst Precursor.
  40. Dehydrative synthesis of chiral oxazolidinones catalyzed by alkali metal carbonates under low pressure of CO2
  41. ChemInform Abstract: The Dual Role of Ruthenium and Alkali Base Catalysts in Enabling a Conceptually New Shortcut to N-Unsubstituted Pyrroles Through Unmasked α-Amino Aldehydes.
  42. ChemInform Abstract: Acetals of N,N-Dimethylformamides: Ambiphilic Behavior in Converting Carbon Dioxide to Dialkyl Carbonates.
  43. Redox-Selective Generation of Aldehydes and H2from Alcohols under Visible Light
  44. Catalytic hydrogenation of unactivated amides enabled by hydrogenation of catalyst precursor
  45. The Dual Role of Ruthenium and Alkali Base Catalysts in Enabling a Conceptually New Shortcut to N -Unsubstituted Pyrroles through Unmasked α-Amino Aldehydes
  46. ChemInform Abstract: Aldol Condensation of Amides Using Phosphazene-Based Catalysis.
  47. Acetals of N,N-Dimethylformamides: Ambiphilic Behavior in Converting Carbon Dioxide to Dialkyl Carbonates
  48. Reaction of an “Invisible” Frustrated N/B Lewis Pair with Dihydrogen
  49. Aldol condensation of amides using phosphazene-based catalysis
  50. ChemInform Abstract: Double Molecular Recognition with Aminoorganoboron Complexes: Selective Alcoholysis of β-Dicarbonyl Derivatives.
  51. Double Molecular Recognition with Aminoorganoboron Complexes: Selective Alcoholysis of β-Dicarbonyl Derivatives
  52. Double Molecular Recognition with Aminoorganoboron Complexes: Selective Alcoholysis of β-Dicarbonyl Derivatives
  53. ChemInform Abstract: CuI/H2/NaOH-Catalyzed Cross-Coupling of Two Different Alcohols for Carbon-Carbon Bond Formation: “Borrowing Hydrogen”?
  54. ChemInform Abstract: One-Pot Nitrile Aldolization/Hydration Operation Giving β-Hydroxy Carboxamides.
  55. Selective N-Alkylation of Amines with Alcohols by Using Non-Metal-Based Acid-Base Cooperative Catalysis
  56. CuI/H2/NaOH-Catalyzed Cross-Coupling of Two Different Alcohols for Carbon-Carbon Bond Formation: “Borrowing Hydrogen”?
  57. ChemInform Abstract: Iron/Amino Acid Catalyzed Direct N-Alkylation of Amines with Alcohols.
  58. ChemInform Abstract: Synthesis of Carbonates Directly from 1 atm CO2 and Alcohols Using CH2Cl2.
  59. One-Pot Nitrile Aldolization/Hydration Operation Giving β-Hydroxy Carboxamides
  60. Iron/Amino Acid Catalyzed Direct N-Alkylation of Amines with Alcohols
  61. Iron/Amino Acid Catalyzed Direct N-Alkylation of Amines with Alcohols
  62. Synthesis of carbonates directly from 1 atm CO2 and alcohols using CH2Cl2
  63. ChemInform Abstract: Efficient Conjugate Reduction of α,β-Unsaturated Carbonyl Compounds by Complexation with Aluminum Tris(2,6-diphenylphenoxide).
  64. ChemInform Abstract: 2,6-Bis(2-alkylphenyl)-3,5-dimethylphenol as a New Chiral Phenol with C2-Symmetry. Application to the Asymmetric Alkylation of Aldehydes.
  65. ChemInform Abstract: Cross-Coupling Reaction of Alcohols for Carbon-Carbon Bond Formation Using Pincer-Type NHC/Palladium Catalysts.
  66. ChemInform Abstract: Conceptually New Directed Aldol Condensation Using Aluminum Tris(2,6-diphenylphenoxide).
  67. ChemInform Abstract: Aluminum Trisphenoxide Polymer as a Lewis Acidic, Solid Catalyst.
  68. ChemInform Abstract: Designer Lewis Acids for Selective Organic Synthesis
  69. ChemInform Abstract: Conjugate Addition of Lithium Enolates to Aromatic Carbonyl Compounds Complexed with Aluminum Tris(2,6-diphenylphenoxide) (ATPH).
  70. ChemInform Abstract: Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary.
  71. ChemInform Abstract: Mixed Crossed Aldol Condensation Between Conjugated Esters and Aldehydes Using Aluminum Tris(2,6-diphenylphenoxide).
  72. ChemInform Abstract: Novel Three Component Coupling of Ketone, Cyclic Ether and Epoxide Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH).
  73. ChemInform Abstract: Designer Lewis Acid Catalysts for Selective Organic Synthesis
  74. ChemInform Abstract: Asymmetric Coupling of Phenols with Arylleads.
  75. ChemInform Abstract: Aluminum Tris(2,6-diphenylphenoxide)-ArCOCl Complex for Nucleophilic Dearomatic Functionalization.
  76. ChemInform Abstract: Asymmetric Mannich-Type Reactions with a Chiral Acetate: Effect of Lewis Acid on Activation of Aldimine.
  77. ChemInform Abstract: Molecular Recognition of Carbonyl Compounds Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): New Regio- and Stereoselective Alkylation of α,β-Unsaturated Carbonyl Compounds
  78. ChemInform Abstract: Diamine-Protonic Acid Catalysts for Catalytic Asymmetric Aldol Reaction.
  79. ChemInform Abstract: Novel Three-Component Coupling Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): The Same Synthetic Strategy Leads to trans- and cis-Jasmonates.
  80. ChemInform Abstract: Nucleophilic Addition of Organomagnesiums to Aldimines: Scandium Triflate (Sc(OTf)3) as an Effective Catalyst.
  81. ChemInform Abstract: Efficient Dehydration of Hydroxyenals and -enones: HfCl4×(THF)2 as an Effective Catalyst for Di-, Tri- and Tetraene Formation.
  82. ChemInform Abstract: Li(I), Na(I), and K(I) Lewis Acids
  83. ChemInform Abstract: Asymmetric Carbon-Carbon Coupling of Phenols or Anilines with Aryllead Triacetates
  84. ChemInform Abstract: Synthesis of a Silanol-Substituted Proline Analogue as Organocatalyst.
  85. Well-elaborated Pd complex catalyst for C–C bond formation
  86. Importance of Open Structure of Nonmetal Based Catalyst in Hydrogen Bond Promoted Methanolysis of Activated Amide: Structure Dynamics between Monomer and Dimer Enabling Recombinant Covalent, Dative, and Hydrogen Bonds
  87. ChemInform Abstract: Aqua-aminoorganoboron Catalyst: Engineering Single Water Molecule to Act as an Acid Catalyst in Nitro Aldol Reaction.
  88. ChemInform Abstract: Development of Organocatalysis Based on the Molecular Design of Pyrrolidine-Broensted Acid Catalysts
  89. Synthesis of 1,4-Diazabicyclo[3.3.1]nonan-6-ones
  90. Methylaluminum Bis(2,6-di-t-butylphenoxide)
  91. ChemInform Abstract: RhI-Catalyzed Aldol-Type Reaction of Organonitriles under Mild Conditions.
  92. ChemInform Abstract: Rh(I)-Catalyzed Hydration of Organonitriles under Ambient Conditions.
  93. RhI-Catalyzed Hydration of Organonitriles under Ambient Conditions
  94. RhI-Catalyzed Hydration of Organonitriles under Ambient Conditions
  95. RhI-catalyzed aldol-type reaction of organonitriles under mild conditions
  96. Aqua-aminoorganoboron Catalyst: Engineering Single Water Molecule to Act as an Acid Catalyst in Nitro Aldol Reaction
  97. ピロリジン‐ブレンステッド酸の分子設計に基づく有機分子触媒反応の開発
  98. Triethylaluminum
  99. Trimethylaluminum
  100. Triethylaluminum
  101. Trimethylaluminum
  102. Methylaluminum Bis(2,6-diphenylphenoxide)
  103. Methylaluminum Bis(2,4,6-tri-tert-butylphenoxide)
  104. Methylaluminum Bis(4-bromo-2,6-di-tert-butylphenoxide)
  105. Methylaluminum Bis(2,6-di-tert-butyl-4-methylphenoxide)
  106. Lead in Organic Synthesis
  107. Aluminum in Organic Synthesis
  108. Lead in Organic Synthesis
  109. Aluminum in Organic Synthesis
  110. Design of Acid—Base Catalysis for the Asymmetric Direct Aldol Reaction
  111. Asymmetric Direct Aldol Reaction Assisted by Water and a Proline-Derived Tetrazole Catalyst.
  112. Design of Acid−Base Catalysis for the Asymmetric Direct Aldol Reaction
  113. Asymmetric Vinylogous Direct Aldol Reaction Using Aluminum Tris[2,6-bis(4-alkylphenyl)phenoxide].
  114. Chiral Molecular Recognition by Aluminum Tris(2,6-diphenylphenoxide) in an Asymmetric 1,4-Addition.
  115. A New Method for the Preparation of Aluminum and Titanium Tris(2,6-diphenylphenoxide) Reagents and Their Application in Organic Synthesis.
  116. O -nitroso aldol synthesis: Catalytic enantioselective route to α-aminooxy carbonyl compounds via enamine intermediate
  117. Asymmetric Direct Aldol Reaction Assisted by Water and a Proline-Derived Tetrazole Catalyst
  118. Asymmetric Direct Aldol Reaction Assisted by Water and a Proline-Derived Tetrazole Catalyst
  119. Chiral Molecular Recognition by Aluminum Tris(2,6-diphenylphenoxide) in an Asymmetric 1,4-Addition
  120. Chiral Molecular Recognition by Aluminum Tris(2,6-diphenylphenoxide) in an Asymmetric 1,4-Addition
  121. Asymmetric Vinylogous Direct Aldol Reaction Using Aluminum Tris[2,6-bis(4-alkylphenyl)phenoxide]
  122. Molecular Recognition of α,β-Unsaturated Carbonyl Compounds Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH):  Structural and Conformational Analysis of ATPH Complexes and Application to the Selective Vinylogous Aldol Reaction
  123. Diversity-Based Strategy for Discovery of Environmentally Benign Organocatalyst: Diamine—Protonic Acid Catalysts for Asymmetric Direct Aldol Reaction.
  124. A New Method for the Preparation of Aluminum and Titanium Tris(2,6-diphenylphenoxide) Reagents and Their Application in Organic Synthesis
  125. Diversity-based strategy for discovery of environmentally benign organocatalyst: diamine–protonic acid catalysts for asymmetric direct aldol reaction
  126. Asymmetric Carbon−Carbon Coupling of Phenols or Anilines with Aryllead Triacetates
  127. Novel Three-Component Coupling Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): The Same Synthetic Strategy Leads totrans- andcis-Jasmonates
  128. Novel Three-Component Coupling Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): The Same Synthetic Strategy Leads to trans- and cis-Jasmonates
  129. ChemInform Abstract: Direct Coupling of Anilines with Aryllead Triacetates.
  130. Diamine-Protonic Acid Catalysts for Catalytic Asymmetric Aldol Reaction
  131. Nucleophilic Addition of Organomagnesiums to Aldimines: Scandium Triflate (Sc(OTf)3) as an Effective Catalyst
  132. Efficient Dehydration of Hydroxyenals and -enones: HfCl4 · (THF)2 as an effective Catalyst for Di-, Tri- and Tetraene Formation
  133. Asymmetric Mannich-type reactions with a chiral acetate: effect of Lewis acid on activation of aldimine
  134. ChemInform Abstract: Molecular Recognition of Carbonyl Compounds Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): New Regio- and Stereoselective Alkylation of α,β-Unsaturated Carbonyl Compounds.
  135. ChemInform Abstract: Regio- and Enantioselective Siloxybutylation at the More Hindered α-Site of Unsymmetrical Ketone Using Chiral Aluminum Trisnaphthoxide.
  136. ChemInform Abstract: Asymmetric Mannich-Type Reactions of Aldimines with a Chiral Acetate.
  137. ChemInform Abstract: Designer Lewis Acids for Selective Organic Synthesis
  138. Aluminum Tris(2,6-diphenylphenoxide)-ArCOCl Complex for Nucleophilic Dearomatic Functionalization
  139. Molecular Recognition of Carbonyl Compounds Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): New Regio- and Stereoselective Alkylation of α,β-Unsaturated Carbonyl Compounds
  140. Asymmetric Mannich-Type Reactions of Aldimines with a Chiral Acetate
  141. Direct Coupling of Anilines with Aryllead Triacetates
  142. Asymmetric Coupling of Phenols with Arylleads
  143. Directed Aldol Condensation
  144. Directed Aldol Condensation
  145. Gemischte Aldol-Kreuzkondensation zwischen konjugierten Estern und Aldehyden mit Aluminiumtris(2,6-diphenylphenoxid)
  146. Gemischte Aldol-Kreuzkondensation zwischen konjugierten Estern und Aldehyden mit Aluminiumtris(2,6-diphenylphenoxid)
  147. Mixed Crossed Aldol Condensation between Conjugated Esters and Aldehydes Using Aluminum Tris(2,6-diphenylphenoxide)
  148. Novel Three Component Coupling of Ketone, Cyclic Ether and Epoxide using Aluminum Tris(2,6-diphenylphenoxide) (ATPH)
  149. Aluminum Trisphenoxide Polymer as a Lewis Acidic, Solid Catalyst
  150. Conjugate Addition of Lithium Enolates to Aromatic Carbonyl Compounds Complexed with Aluminum Tris(2,6-diphenylphenoxide) (ATPH)
  151. Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary
  152. Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary
  153. Diastereoselektive Aldolreaktion mit einem Acetat-Enolat: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol als äußerst effektives chirales Auxiliar
  154. Conceptually New Directed Aldol Condensation Using Aluminum Tris(2,6-diphenylphenoxide)
  155. 2,6-Bis(2-alkylphenyl)-3,5-dimethylphenol as a New Chiral Phenol with C 2 -Symmetry. Application to the Asymmetric Alkylation of Aldehydes
  156. Selective Alkylation of Ketones with a Bulky Aluminum Reagent-the THF-TBSOTf System
  157. A New Annulation Based on a One-Pot Double Michael Addition Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH)
  158. Designer Lewis acid catalysts—bulky aluminium reagents for selective organic synthesis
  159. A new synthetic route to allylsilanes: the reaction of silyllithium reagents with aromatic carbonyl compounds and aluminium tris(2,6-diphenylphenoxide) (ATPH)
  160. Highly Regioselective Alkylation at the More-Hindered α-Site of Unsymmetrical Ketones by the Combined Use of Aluminum Tris(2,6-diphenylphenoxide) and Lithium Diisopropylamide
  161. Regioselective Robinson Annulation Realized by the Combined Use of Lithium Enolates and Aluminum Tris(2,6-diphenylphenoxide) (ATPH).
  162. Aluminum Tris(4-bromo-2,6-diphenylphenoxide) (ATPH-Br): an Effective Catalyst for Claisen Rearrangement
  163. Efficient Conjugate Reduction of α,β-Unsaturated Carbonyl Compounds by Complexation with Aluminum Tris(2,6-diphenylphenoxide)
  164. Molecular Design of a Chiral Lewis Acid for the Asymmetric Claisen Rearrangement
  165. Asymmetric Diels-Alder Reaction of Unsymmetrical Maleates. A Chemical Access to Chiral, Unsymmetrical cis-Cyclohexene-1,2-dicarboxylates
  166. Virtually Complete Blocking of .alpha.,.beta.-Unsaturated Aldehyde Carbonyls by Complexation with Aluminum Tris(2,6-diphenylphenoxide)
  167. Aluminum Tris(2,6-diphenylphenoxide) (ATPH) as an Extremely Selective Activator of Less Hindered Aldehyde Carbonyls
  168. Chemoselective functionalization of more hindered aldehyde carbonyls with the methylaluminum bis(2,6-diphenylphenoxide)/alkyllithium system
  169. Regiocontrolled [2+2] Cycloaddition of Unsymmetrical Fumarates Based on the Discrimination of Two Different Ester Carbonyls with Methylaluminum Bis(2,6-di- tert -butyl-4-methylphenoxide) (MAD)
  170. Discrimination of two different ester carbonyls with methylaluminum bis(2,6-di-tert-butyl-4-methylphenoxide). Application to the regiocontrolled and stereocontrolled Diels-Alder reaction of unsymmetrical fumarates
  171. Selective Reduction of Methylenecycloalkane Oxides with 4-Substituted Diisobutylaluminum 2,6-Di- tert -butylphenoxides
  172. A New Stereoselective Approach to Oxygenated Carbocycles: Asymmetric Synthesis of the Cyclohexyl Fragment of FK-506
  173. Carbonyl Recognition
  174. Li(I), Na(I), and K(I) Lewis Acids