302 results on '"Qiao, Jennifer X."'
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52. Leveraging a “Catch–Release” Logic Gate Process for the Synthesis and Nonchromatographic Purification of Thioether- or Amine-Bridged Macrocyclic Peptides
53. Decarboxylative alkylation for site-selective bioconjugation of native proteins via oxidation potentials
54. CITU: A Peptide and Decarboxylative Coupling Reagent
55. Palladium(II)-Catalyzed Site-Selective C(sp3 )−H Alkynylation of Oligopeptides: A Linchpin Approach for Oligopeptide-Drug Conjugation
56. Formation of α-chiral centers by asymmetric β-C(sp 3 )–H arylation, alkenylation, and alkynylation
57. PdII‐Catalyzed Enantioselective C(sp3)−H Activation/Cross‐Coupling Reactions of Free Carboxylic Acids.
58. Orally bioavailable factor Xa inhibitors containing alpha-substituted gem-dimethyl P4 moieties
59. 2-Amino-1,3,4-thiadiazoles in the 7-hydroxy-N-neopentyl spiropiperidine indolinyl series as potent P2Y1 receptor antagonists
60. Identification of 1-{2-[4-chloro-1′-(2,2-dimethylpropyl)-7-hydroxy-1,2-dihydrospiro[indole-3,4′-piperidine]-1-yl]phenyl}-3-{5-chloro-[1,3]thiazolo[5,4-b]pyridin-2-yl}urea, a potent, efficacious and orally bioavailable P2Y1 antagonist as an antiplatelet agent
61. Potent P2Y1 urea antagonists bearing various cyclic amine scaffolds
62. Discovery of diarylurea P2Y1 antagonists with improved aqueous solubility
63. Decarboxylative Peptide Macrocyclization through Photoredox Catalysis
64. Synthesis of Fmoc-Protected Arylphenylalanines (Bip Derivatives) via Nonaqueous Suzuki-Miyaura Cross-Coupling Reactions
65. ChemInform Abstract: Microwave-Assisted Transamidation of Ureas.
66. Ligand-Enabled β‑C(sp3)–H Olefination of Free Carboxylic Acids.
67. metaC–H Arylation of Electron-Rich Arenes: Reversing the Conventional Site Selectivity
68. Versatile Copper-Catalyzed γ-C(sp3)–H Lactonization of Aliphatic Acids
69. Leveraging a “Catch–Release” Logic Gate Process for the Synthesis and Nonchromatographic Purification of Thioether- or Amine-Bridged Macrocyclic Peptides
70. Triphenylethanamine Derivatives as Cholesteryl Ester Transfer Protein Inhibitors: Discovery of N-[(1R)-1-(3-Cyclopropoxy-4-fluorophenyl)-1-[3-fluoro-5-(1,1,2,2-tetrafluoroethoxy)phenyl]-2-phenylethyl]-4-fluoro-3-(trifluoromethyl)benzamide (BMS-795311)
71. Palladium(II)-Catalyzed Site-Selective C(sp3)−H Alkynylation of Oligopeptides: A Linchpin Approach for Oligopeptide-Drug Conjugation.
72. Formation of α-chiral centers by asymmetric β-C(sp3)–H arylation, alkenylation, and alkynylation.
73. Discovery of 4-Aryl-7-Hydroxyindoline-Based P2Y1 Antagonists as Novel Antiplatelet Agents
74. 4-Benzothiazole-7-hydroxyindolinyl Diaryl Ureas Are Potent P2Y1Antagonists with Favorable Pharmacokinetics: Low Clearance and Small Volume of Distribution
75. Highly efficacious factor Xa inhibitors containing α-substituted phenylcycloalkyl P4 moieties
76. Conformationally Constrained ortho-Anilino Diaryl Ureas: Discovery of 1-(2-(1′-Neopentylspiro[indoline-3,4′-piperidine]-1-yl)phenyl)-3-(4-(trifluoromethoxy)phenyl)urea, a Potent, Selective, and Bioavailable P2Y1 Antagonist
77. Decarboxylative Peptide Macrocyclization through Photoredox Catalysis.
78. Achieving structural diversity using the perpendicular conformation of alpha-substituted phenylcyclopropanes to mimic the bioactive conformation of ortho-substituted biphenyl P4 moieties: Discovery of novel, highly potent inhibitors of Factor Xa
79. 2-Arylbenzoxazoles as novel cholesteryl ester transfer protein inhibitors: Optimization via array synthesis
80. ChemInform Abstract: Synthesis of Tertiary Carbinamines.
81. Diphenylpyridylethanamine (DPPE) Derivatives as Cholesteryl Ester Transfer Protein (CETP) Inhibitors
82. The emergence of factor Xa inhibitors for the treatment of cardiovascular diseases: a patent review
83. ChemInform Abstract: AlMe3-Promoted Formation of Amides from Acids and Amines.
84. AlMe3-Promoted Formation of Amides from Acids and Amines
85. Recent Advances in Chan–Lam Coupling Reaction: Copper‐Promoted C–Heteroatom Bond Cross‐Coupling Reactions with Boronic Acids and Derivatives
86. ChemInform Abstract: Copper-Promoted Carbon-Heteroatom Bond Cross-Coupling with Boronic Acids and Derivatives
87. ChemInform Abstract: Transformation of Anionically Activated Trifluoromethyl Groups to Heterocycles under Mild Aqueous Conditions.
88. Transformation of Anionically Activated Trifluoromethyl Groups to Heterocycles under Mild Aqueous Conditions
89. SAR and X-ray structures of enantiopure 1,2-cis-(1R,2S)-cyclopentyldiamine and cyclohexyldiamine derivatives as inhibitors of coagulation Factor Xa
90. ChemInform Abstract: Preparation of Monofluorophenols via the Reaction of Difluorobenzene Derivatives with Potassium Trimethylsilanoate.
91. Enantiopure five-membered cyclicdiamine derivatives as potent and selective inhibitors of factor Xa. Improving in vitro metabolic stability via core modifications
92. Pyrazole-based factor Xa inhibitors containing N-arylpiperidinyl P4 residues
93. A practical synthesis of aryl tetrafluoroethyl ethers via the improved reaction of phenols with 1,2-dibromotetrafluoroethane
94. 5-Amidinoindoles as Dual Inhibitors of Coagulation Factors IXa and Xa.
95. 5-Amidinobenzo[b]thiophenes as dual inhibitors of factors IXa and Xa
96. 5-Amidinoindoles as dual inhibitors of coagulation factors IXa and Xa
97. 4-Benzothiazole-7-hydroxyindolinyl Diaryl Ureas Are Potent P2Y1 Antagonists with Favorable Pharmacokinetics: Low Clearance and Small Volume of Distribution.
98. Discovery of 4-Aryl-7-Hydroxyindoline-Based P2Y1Antagonists as NovelAntiplatelet Agents.
99. 5-Amidinobenzo[ b]thiophenes as dual inhibitors of factors IXa and Xa
100. Conformationally Constrained ortho-Anilino Diaryl Ureas: Discovery of 1-(2-(1′-Neopentylspiro[indoline-3,4′-piperidine]-1-yl)phenyl)-3-(4-(trifluoromethoxy)phenyl)urea,a Potent, Selective, and Bioavailable P2Y1Antagonist.
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