424 results on '"Song, Jinhua J."'
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52. ChemInform Abstract: Efficient Iron-Catalyzed Kumada Cross-Coupling Reactions Utilizing Flow Technology under Low Catalyst Loadings.
53. Rhodium-Catalyzed Asymmetric Allenylation of Sulfonylimines and Application to the Stereospecific Allylic Allenylation
54. ChemInform Abstract: Synthesis of P-Chiral Dihydrobenzooxaphospholes Through Negishi Cross-Coupling.
55. Efficient Iron-Catalyzed Kumada Cross-Coupling Reactions Utilizing Flow Technology under Low Catalyst Loadings
56. Enantioselective Arylation of Oxindoles Using Modified BI-DIME Ligands.
57. Modular Dihydrobenzoazaphosphole Ligands for Suzuki-Miyaura Cross-Coupling.
58. BABIPhos Family of Biaryl Dihydrobenzooxaphosphole Ligands for Asymmetric Hydrogenation.
59. Enantioselective Synthesis of α-(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights.
60. Early Development Scale-Up of a Structurally-Challenging 5-Lipoxygenase Activating Protein (FLAP) Inhibitor
61. Enantioselective Synthesis of α-(Hetero)aryl Piperidines through Asymmetric Hydrogenation of Pyridinium Salts and Its Mechanistic Insights
62. Nickel-catalyzed C-3 direct arylation of pyridinium ions for the synthesis of 1-azafluorenes
63. Synthesis of P-Chiral Dihydrobenzooxaphospholes Through Negishi Cross-Coupling
64. Development of an Efficient Synthesis of (2-Aminopyrimidin-5-yl) Boronic Acid
65. Development of a Practical Sequence for Difluoromethylation of 2-Bromopyridines via Copper-Mediated Reductive Coupling and Decarboxylation
66. Synthesis of two potent glucocorticoid receptor agonists labeled with carbon-14 and stable isotopes
67. Efficient Asymmetric Synthesis of Structurally Diverse P-Stereogenic Phosphinamides for Catalyst Design
68. Development of an Asymmetric Synthesis of a Chiral Quaternary FLAP Inhibitor
69. Synthesis of p38 MAP kinase inhibitor BIRB 796 and analogs via copper-mediated N-arylation reaction
70. ChemInform Abstract: General and Rapid Pyrimidine Condensation by Addressing the Rate Limiting Aromatization.
71. A Mild Dihydrobenzooxaphosphole Oxazoline/Iridium Catalytic System for Asymmetric Hydrogenation of Unfunctionalized Dialins
72. Development of New P-Chiral P,π-Dihydrobenzooxaphosphole Hybrid Ligands for Asymmetric Catalysis
73. Synthesis of empagliflozin, a novel and selective sodium-glucose co-transporter-2 inhibitor, labeled with carbon-14 and carbon-13
74. Remarkable Enhancement of Enantioselectivity in the Asymmetric Conjugate Addition of Dimethylzinc to (Z)‐Nitroalkenes with a Catalytic [(MeCN)4Cu]PF6–Hoveyda Ligand Complex
75. Addressing the Configuration Stability of Lithiated Secondary Benzylic Carbamates for the Development of a Noncryogenic Stereospecific Boronate Rearrangement
76. Facile Entry to an Efficient and Practical Enantioselective Synthesis of a Polycyclic Cholesteryl Ester Transfer Protein Inhibitor
77. Development of an Enantioselective Hydrogenation Route to (S)-1-(2-(Methylsulfonyl)pyridin-4-yl)propan-1-amine
78. General and Rapid Pyrimidine Condensation by Addressing the Rate Limiting Aromatization
79. Challenges and Opportunities for Scaling the Ring‐Closing Metathesis Reaction in the Pharmaceutical Industry
80. A Scalable and Regioselective Synthesis of 2-Difluoromethyl Pyridines from Commodity Chemicals
81. One-step construction of 2-substituted-4,6-diazaindoles from carboxylic acid derivatives
82. Acid-promoted S N1/E1 fragmentation/dimerization of 2-cumylmalonates
83. Application of newly developed anti-selective aldol methodology: synthesis of C6-C13 and C19-C28 fragments of miyakolide
84. Synthesis of Trifluoromethyl Ketones from Carboxylic Acids: 4-(3,4-Dibromophenyl)-1,1,1-trifluoro-4-methylpentan-2-one
85. Synthesis of Pyridyl-dihydrobenzooxaphosphole Ligands and Their Application in Asymmetric Hydrogenation of Unfunctionalized Alkenes
86. Design and Synthesis of Chiral Oxathiozinone Scaffolds: Efficient Synthesis of Hindered Enantiopure Sulfinamides and Sulfinyl Ketimines
87. Development of a Safe and Economical Synthesis of Methyl 6-Chloro-5-(trifluoromethyl)nicotinate: Trifluoromethylation on Kilogram Scale
88. Heart-Cutting Two-Dimensional Ultrahigh-Pressure Liquid Chromatography for Process Development: Asymmetric Reaction Monitoring
89. Zinc Catalyzed and Mediated Asymmetric Propargylation of Trifluoromethyl Ketones with a Propargyl Boronate
90. Development of a Large Scale Asymmetric Synthesis of the Glucocorticoid Agonist BI 653048 BS H3PO4
91. ChemInform Abstract: Transition Metal Catalysis in the Pharmaceutical Industry
92. Asymmetric Methallylation of Ketones Catalyzed by a Highly Active Organocatalyst 3,3′-F2-BINOL
93. Synthesis of Enantioenriched 2-Alkyl Piperidine Derivatives through Asymmetric Reduction of Pyridinium Salts.
94. Efficient Iron-Catalyzed Kumada Cross-Coupling Reactions Utilizing Flow Technology under Low Catalyst Loadings.
95. Development and Characterization of a Cocrystal as a Viable Solid Form for an Active Pharmaceutical Ingredient
96. Efficient Asymmetric Synthesis of P-Chiral Phosphine Oxides via Properly Designed and Activated Benzoxazaphosphinine-2-oxide Agents
97. The Eight Criteria Defining a Good Chemical Manufacturing Process
98. Transition Metal Catalysis in the Pharmaceutical Industry
99. ChemInform Abstract: Zinc‐Catalyzed Allenylations of Aldehydes and Ketones.
100. Preparative Synthesis via Continuous Flow of 4,4,5,5-Tetramethyl-2-(3-trimethylsilyl-2-propynyl)-1,3,2-dioxaborolane: A General Propargylation Reagent
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