All Stories

  1. Hydrogenation of CO2 to MeOH Catalyzed by Highly Robust (PNNP)Ir Complexes Activated by Alkali Bases in Alcohol
  2. N‐Methylation of Twenty Different α‐Amino Acid Motifs Using Methanol under Metal‐Loaded Titanium Dioxide Photocatalysis
  3. Metal-Loaded Semiconductor-Photocatalysis of Alcohols for Selective Organic Synthesis: A Personal Account
  4. Machine‐Learning Classification for the Prediction of Catalytic Activity of Organic Photosensitizers in the Nickel(II)‐Salt‐Induced Synthesis of Phenols
  5. Sustainable organic synthesis promoted on titanium dioxide using coordinated water and renewable energies/resources
  6. Arylamines as More Strongly Reducing Organic Photoredox Catalysts than fac-[Ir(ppy)3]
  7. Photocatalytic CO2 Reduction Using an Iron–Bipyridyl Complex Supported by Two Phosphines for Improving Catalyst Durability
  8. Selective Reduction of Carboxylic Acids to Alcohols in the Presence of Alcohols by a Dual Bulky Transition-Metal Complex/Lewis Acid Catalyst
  9. Bulkiness of catalyst for photocatalytic CO2 reduction
  10. Phosphorus-Based Organocatalysis for the Dehydrative Cyclization of N-(2-Hydroxyethyl)amides into 2-Oxazolines
  11. ruthenium catalyst for CO2 photo-reduction
  12. CO2 as C1 source for photocatalytic C–C bond formation
  13. Development of Effective Bidentate Diphosphine Ligands of Ruthenium Catalysts toward Practical Hydrogenation of Carboxylic Acids
  14. C(sp3)–H bond functionalization with styrenes via hydrogen-atom transfer to an aqueous hydroxyl radical under photocatalysis
  15. Preparation of a platinum nanoparticle catalyst located near photocatalyst titanium oxide and its catalytic activity to convert benzyl alcohols to the corresponding ethers
  16. Catalyzing a Zero-Carbon World by Harvesting Energy from Living Cells
  17. catechol-coordinated P(V) for dehydrate amide bond formation
  18. A single, mononuclear Ir complex for CO2 photoreduction
  19. natural amino acids goes to beta-amino alcohols
  20. Amine gives secondary amine and NH3
  21. So many drugs have N-methyl and N-ethyl units. Using alcohols, how we could synthesize drugs?
  22. One boron or two-connected borons, which would be better for amide bond formation?
  23. Interplay of Cu and Au, immobilized on TiO2 (P25) for N-alkylation under light!
  24. carboxylic acids (CAs) and their reduced form alcohols are renewables, going to SDGs!!
  25. Light energy for synthesizing propylene and fragrance lavandulol from renewable resources
  26. Trimethylaluminum
  27. High valent metal complex turns catalysis on its head for a sustainable future
  28. Ruthenium catalyst breaks down plastic wastes by hydrogenation
  29. Dehydrogenation of Primary Aliphatic Alcohols by Au/TiO2 Photocatalysts
  30. Synthesis of morphan derivatives with additional substituents in 8-position
  31. (PN)2Ru complexes for hydrogen attachment and detachment
  32. Investigation of the Corey Bromolactamization withN-Functionalized Allylamines
  33. Milestone discovery: molecular catalyst design for hydrogenation of carboxylic acids (CAs)
  34. N-Methylation of Amines with Methanol at Room Temperature
  35. Stereoselective Synthesis ofcis,cis-Configured Perhydroquinoxaline-5-Carbonitrile from Cyclohex-2-en-1-ol
  36. ChemInform Abstract: Catalytic Fluoride Triggers Dehydrative Oxazolidinone Synthesis from CO2.
  37. ChemInform Abstract: Stereoselective Synthesis of cis,cis-Configured Vicinal Triamines.
  38. One-step synthesis of patterned polymer brushes by photocatalytic microcontact printing
  39. Hydration of nitriles to amides by a chitin-supported ruthenium catalyst
  40. Catalytic fluoride triggers dehydrative oxazolidinone synthesis from CO2
  41. Stereoselective Synthesis ofcis,cis-Configured Vicinal Triamines
  42. Bromolactamization: Key Step in the Stereoselective Synthesis of Enantiomerically Pure, cis -Configured Perhydropyrroloquinoxalines
  43. Synthesis of propylene from renewable allyl alcohol by photocatalytic transfer hydrogenolysis
  44. ChemInform Abstract: Dehydrative Synthesis of Chiral Oxazolidinones Catalyzed by Alkali Metal Carbonates under Low Pressure of CO2.
  45. ChemInform Abstract: Catalytic Hydrogenation of Unactivated Amides Enabled by Hydrogenation of Catalyst Precursor.
  46. Dehydrative synthesis of chiral oxazolidinones catalyzed by alkali metal carbonates under low pressure of CO2
  47. 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.
  48. ChemInform Abstract: Acetals of N,N-Dimethylformamides: Ambiphilic Behavior in Converting Carbon Dioxide to Dialkyl Carbonates.
  49. Redox-Selective Generation of Aldehydes and H2from Alcohols under Visible Light
  50. Catalytic hydrogenation of unactivated amides enabled by hydrogenation of catalyst precursor
  51. The Dual Role of Ruthenium and Alkali Base Catalysts in Enabling a Conceptually New Shortcut to N -Unsubstituted Pyrroles through Unmasked α-Amino Aldehydes
  52. ChemInform Abstract: Aldol Condensation of Amides Using Phosphazene-Based Catalysis.
  53. Acetals of N,N-Dimethylformamides: Ambiphilic Behavior in Converting Carbon Dioxide to Dialkyl Carbonates
  54. Reaction of an “Invisible” Frustrated N/B Lewis Pair with Dihydrogen
  55. Aldol condensation of amides using phosphazene-based catalysis
  56. ChemInform Abstract: Double Molecular Recognition with Aminoorganoboron Complexes: Selective Alcoholysis of β-Dicarbonyl Derivatives.
  57. Double Molecular Recognition with Aminoorganoboron Complexes: Selective Alcoholysis of β-Dicarbonyl Derivatives
  58. Double Molecular Recognition with Aminoorganoboron Complexes: Selective Alcoholysis of β-Dicarbonyl Derivatives
  59. ChemInform Abstract: CuI/H2/NaOH-Catalyzed Cross-Coupling of Two Different Alcohols for Carbon-Carbon Bond Formation: “Borrowing Hydrogen”?
  60. ChemInform Abstract: One-Pot Nitrile Aldolization/Hydration Operation Giving β-Hydroxy Carboxamides.
  61. Selective N-Alkylation of Amines with Alcohols by Using Non-Metal-Based Acid-Base Cooperative Catalysis
  62. CuI/H2/NaOH-Catalyzed Cross-Coupling of Two Different Alcohols for Carbon-Carbon Bond Formation: “Borrowing Hydrogen”?
  63. ChemInform Abstract: Iron/Amino Acid Catalyzed Direct N‐Alkylation of Amines with Alcohols.
  64. ChemInform Abstract: Synthesis of Carbonates Directly from 1 atm CO2 and Alcohols Using CH2Cl2.
  65. One-Pot Nitrile Aldolization/Hydration Operation Giving β-Hydroxy Carboxamides
  66. Iron/Amino Acid Catalyzed Direct N‐Alkylation of Amines with Alcohols
  67. Iron/Amino Acid Catalyzed Direct N-Alkylation of Amines with Alcohols
  68. Synthesis of carbonates directly from 1 atm CO2 and alcohols using CH2Cl2
  69. ChemInform Abstract: Efficient Conjugate Reduction of α,β-Unsaturated Carbonyl Compounds by Complexation with Aluminum Tris(2,6-diphenylphenoxide).
  70. 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.
  71. ChemInform Abstract: Cross-Coupling Reaction of Alcohols for Carbon-Carbon Bond Formation Using Pincer-Type NHC/Palladium Catalysts.
  72. ChemInform Abstract: Conceptually New Directed Aldol Condensation Using Aluminum Tris(2,6-diphenylphenoxide).
  73. ChemInform Abstract: Aluminum Trisphenoxide Polymer as a Lewis Acidic, Solid Catalyst.
  74. ChemInform Abstract: Designer Lewis Acids for Selective Organic Synthesis
  75. ChemInform Abstract: Conjugate Addition of Lithium Enolates to Aromatic Carbonyl Compounds Complexed with Aluminum Tris(2,6-diphenylphenoxide) (ATPH).
  76. ChemInform Abstract: Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary.
  77. ChemInform Abstract: Mixed Crossed Aldol Condensation Between Conjugated Esters and Aldehydes Using Aluminum Tris(2,6-diphenylphenoxide).
  78. ChemInform Abstract: Novel Three Component Coupling of Ketone, Cyclic Ether and Epoxide Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH).
  79. ChemInform Abstract: Designer Lewis Acid Catalysts for Selective Organic Synthesis
  80. ChemInform Abstract: Asymmetric Coupling of Phenols with Arylleads.
  81. ChemInform Abstract: Aluminum Tris(2,6-diphenylphenoxide)-ArCOCl Complex for Nucleophilic Dearomatic Functionalization.
  82. ChemInform Abstract: Asymmetric Mannich-Type Reactions with a Chiral Acetate: Effect of Lewis Acid on Activation of Aldimine.
  83. 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
  84. ChemInform Abstract: Diamine-Protonic Acid Catalysts for Catalytic Asymmetric Aldol Reaction.
  85. ChemInform Abstract: Novel Three-Component Coupling Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): The Same Synthetic Strategy Leads to trans- and cis-Jasmonates.
  86. ChemInform Abstract: Nucleophilic Addition of Organomagnesiums to Aldimines: Scandium Triflate (Sc(OTf)3) as an Effective Catalyst.
  87. ChemInform Abstract: Efficient Dehydration of Hydroxyenals and -enones: HfCl4×(THF)2 as an Effective Catalyst for Di-, Tri- and Tetraene Formation.
  88. ChemInform Abstract: Li(I), Na(I), and K(I) Lewis Acids
  89. ChemInform Abstract: Asymmetric Carbon-Carbon Coupling of Phenols or Anilines with Aryllead Triacetates
  90. ChemInform Abstract: Synthesis of a Silanol-Substituted Proline Analogue as Organocatalyst.
  91. Well-elaborated Pd complex catalyst for C–C bond formation
  92. 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
  93. ChemInform Abstract: Aqua-aminoorganoboron Catalyst: Engineering Single Water Molecule to Act as an Acid Catalyst in Nitro Aldol Reaction.
  94. ChemInform Abstract: Development of Organocatalysis Based on the Molecular Design of Pyrrolidine-Broensted Acid Catalysts
  95. Synthesis of 1,4-Diazabicyclo[3.3.1]nonan-6-ones
  96. Methylaluminum Bis(2,6-di-t-butylphenoxide)
  97. ChemInform Abstract: RhI-Catalyzed Aldol-Type Reaction of Organonitriles under Mild Conditions.
  98. ChemInform Abstract: Rh(I)-Catalyzed Hydration of Organonitriles under Ambient Conditions.
  99. RhI-Catalyzed Hydration of Organonitriles under Ambient Conditions
  100. RhI-Catalyzed Hydration of Organonitriles under Ambient Conditions
  101. RhI-catalyzed aldol-type reaction of organonitriles under mild conditions
  102. Aqua-aminoorganoboron Catalyst: Engineering Single Water Molecule to Act as an Acid Catalyst in Nitro Aldol Reaction
  103. 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
  104. Triethylaluminum
  105. Trimethylaluminum
  106. Triethylaluminum
  107. Trimethylaluminum
  108. Methylaluminum Bis(2,6-diphenylphenoxide)
  109. Methylaluminum Bis(2,4,6-tri-tert-butylphenoxide)
  110. Methylaluminum Bis(4-bromo-2,6-di-tert-butylphenoxide)
  111. Methylaluminum Bis(2,6-di-tert-butyl-4-methylphenoxide)
  112. Lead in Organic Synthesis
  113. Aluminum in Organic Synthesis
  114. Lead in Organic Synthesis
  115. Aluminum in Organic Synthesis
  116. Design of Acid—Base Catalysis for the Asymmetric Direct Aldol Reaction
  117. Asymmetric Direct Aldol Reaction Assisted by Water and a Proline-Derived Tetrazole Catalyst.
  118. Design of Acid−Base Catalysis for the Asymmetric Direct Aldol Reaction
  119. Asymmetric Vinylogous Direct Aldol Reaction Using Aluminum Tris[2,6-bis(4-alkylphenyl)phenoxide].
  120. Chiral Molecular Recognition by Aluminum Tris(2,6-diphenylphenoxide) in an Asymmetric 1,4-Addition.
  121. A New Method for the Preparation of Aluminum and Titanium Tris(2,6-diphenylphenoxide) Reagents and Their Application in Organic Synthesis.
  122. O -nitroso aldol synthesis: Catalytic enantioselective route to α-aminooxy carbonyl compounds via enamine intermediate
  123. Asymmetric Direct Aldol Reaction Assisted by Water and a Proline-Derived Tetrazole Catalyst
  124. Asymmetric Direct Aldol Reaction Assisted by Water and a Proline-Derived Tetrazole Catalyst
  125. Chiral Molecular Recognition by Aluminum Tris(2,6-diphenylphenoxide) in an Asymmetric 1,4-Addition
  126. Chiral Molecular Recognition by Aluminum Tris(2,6-diphenylphenoxide) in an Asymmetric 1,4-Addition
  127. Asymmetric Vinylogous Direct Aldol Reaction Using Aluminum Tris[2,6-bis(4-alkylphenyl)phenoxide]
  128. 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
  129. Diversity-Based Strategy for Discovery of Environmentally Benign Organocatalyst: Diamine—Protonic Acid Catalysts for Asymmetric Direct Aldol Reaction.
  130. A New Method for the Preparation of Aluminum and Titanium Tris(2,6-diphenylphenoxide) Reagents and Their Application in Organic Synthesis
  131. Diversity-based strategy for discovery of environmentally benign organocatalyst: diamine–protonic acid catalysts for asymmetric direct aldol reaction
  132. Asymmetric Carbon−Carbon Coupling of Phenols or Anilines with Aryllead Triacetates
  133. Novel Three-Component Coupling Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): The Same Synthetic Strategy Leads totrans- andcis-Jasmonates
  134. Novel Three-Component Coupling Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): The Same Synthetic Strategy Leads to trans- and cis-Jasmonates
  135. ChemInform Abstract: Direct Coupling of Anilines with Aryllead Triacetates.
  136. Diamine-Protonic Acid Catalysts for Catalytic Asymmetric Aldol Reaction
  137. Nucleophilic Addition of Organomagnesiums to Aldimines: Scandium Triflate (Sc(OTf)3) as an Effective Catalyst
  138. Efficient Dehydration of Hydroxyenals and -enones: HfCl4 · (THF)2 as an effective Catalyst for Di-, Tri- and Tetraene Formation
  139. Asymmetric Mannich-type reactions with a chiral acetate: effect of Lewis acid on activation of aldimine
  140. 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.
  141. ChemInform Abstract: Regio- and Enantioselective Siloxybutylation at the More Hindered α-Site of Unsymmetrical Ketone Using Chiral Aluminum Trisnaphthoxide.
  142. ChemInform Abstract: Asymmetric Mannich-Type Reactions of Aldimines with a Chiral Acetate.
  143. ChemInform Abstract: Designer Lewis Acids for Selective Organic Synthesis
  144. Aluminum Tris(2,6-diphenylphenoxide)-ArCOCl Complex for Nucleophilic Dearomatic Functionalization
  145. Molecular Recognition of Carbonyl Compounds Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH): New Regio- and Stereoselective Alkylation of α,β-Unsaturated Carbonyl Compounds
  146. Asymmetric Mannich-Type Reactions of Aldimines with a Chiral Acetate
  147. Direct Coupling of Anilines with Aryllead Triacetates
  148. Asymmetric Coupling of Phenols with Arylleads
  149. Directed Aldol Condensation
  150. Directed Aldol Condensation
  151. Gemischte Aldol-Kreuzkondensation zwischen konjugierten Estern und Aldehyden mit Aluminiumtris(2,6-diphenylphenoxid)
  152. Gemischte Aldol-Kreuzkondensation zwischen konjugierten Estern und Aldehyden mit Aluminiumtris(2,6-diphenylphenoxid)
  153. Mixed Crossed Aldol Condensation between Conjugated Esters and Aldehydes Using Aluminum Tris(2,6-diphenylphenoxide)
  154. Novel Three Component Coupling of Ketone, Cyclic Ether and Epoxide using Aluminum Tris(2,6-diphenylphenoxide) (ATPH)
  155. Aluminum Trisphenoxide Polymer as a Lewis Acidic, Solid Catalyst
  156. Conjugate Addition of Lithium Enolates to Aromatic Carbonyl Compounds Complexed with Aluminum Tris(2,6-diphenylphenoxide) (ATPH)
  157. Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary
  158. Diastereoselective Aldol Reaction with an Acetate Enolate: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol as an Extremely Effective Chiral Auxiliary
  159. Diastereoselektive Aldolreaktion mit einem Acetat-Enolat: 2,6-Bis(2-isopropylphenyl)-3,5-dimethylphenol als äußerst effektives chirales Auxiliar
  160. Conceptually New Directed Aldol Condensation Using Aluminum Tris(2,6-diphenylphenoxide)
  161. 2,6-Bis(2-alkylphenyl)-3,5-dimethylphenol as a New Chiral Phenol with C 2 -Symmetry. Application to the Asymmetric Alkylation of Aldehydes
  162. Selective Alkylation of Ketones with a Bulky Aluminum Reagent-the THF-TBSOTf System
  163. A New Annulation Based on a One-Pot Double Michael Addition Using Aluminum Tris(2,6-diphenylphenoxide) (ATPH)
  164. Designer Lewis acid catalysts—bulky aluminium reagents for selective organic synthesis
  165. A new synthetic route to allylsilanes: the reaction of silyllithium reagents with aromatic carbonyl compounds and aluminium tris(2,6-diphenylphenoxide) (ATPH)
  166. 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
  167. Regioselective Robinson Annulation Realized by the Combined Use of Lithium Enolates and Aluminum Tris(2,6-diphenylphenoxide) (ATPH).
  168. Aluminum Tris(4-bromo-2,6-diphenylphenoxide) (ATPH-Br): an Effective Catalyst for Claisen Rearrangement
  169. Efficient Conjugate Reduction of α,β-Unsaturated Carbonyl Compounds by Complexation with Aluminum Tris(2,6-diphenylphenoxide)
  170. Molecular Design of a Chiral Lewis Acid for the Asymmetric Claisen Rearrangement
  171. Asymmetric Diels-Alder Reaction of Unsymmetrical Maleates. A Chemical Access to Chiral, Unsymmetrical cis-Cyclohexene-1,2-dicarboxylates
  172. Virtually Complete Blocking of .alpha.,.beta.-Unsaturated Aldehyde Carbonyls by Complexation with Aluminum Tris(2,6-diphenylphenoxide)
  173. Aluminum Tris(2,6-diphenylphenoxide) (ATPH) as an Extremely Selective Activator of Less Hindered Aldehyde Carbonyls
  174. Chemoselective functionalization of more hindered aldehyde carbonyls with the methylaluminum bis(2,6-diphenylphenoxide)/alkyllithium system
  175. 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)
  176. 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
  177. Selective Reduction of Methylenecycloalkane Oxides with 4-Substituted Diisobutylaluminum 2,6-Di- tert -butylphenoxides
  178. A New Stereoselective Approach to Oxygenated Carbocycles: Asymmetric Synthesis of the Cyclohexyl Fragment of FK-506
  179. Carbonyl Recognition
  180. Li(I), Na(I), and K(I) Lewis Acids