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An Investigation on the Diastereoselectivity of α-Methylstyrene Cyclopropanations Catalyzed by Dirhodium (II) Catalysts
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Synthesis of Novel Nucleotide Tenofovir/Lamivudine Prodrug Conjugates for treatment of Human Immunodeficiency Virus and Hepatitis B
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Synthesis and Evaluation of Novel Phenyl-Adamantane Dirhodium Catalyst for C-H Functionalization
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New Advances in Asymmetric Cyclopropanation and Drug Discoveries Using Dirhodium(II) Tetracarboxylates
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Asparagine and Glutamine Bioconjugation
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Synthesis of alkyl analogues of 1,4-dihydropyridine for developing novel treatment against chemoresistance in prostate cancer
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Carboxylation of C(sp2) Bromides Enabled by Metallophotoredox Dual Catalysis and Sodium Formate
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Computational Modeling of Oxyradical and Metal-Oxo Reactivity and Selectivity in Hydrogen Atom Transfer Reactions
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Triazene Coarctate Cyclization for the Synthesis of Fluorescent Cyclic Peptides
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Novel Quaternary Ammonium Compounds Derived from the Antimicrobial Natural Product Ianthelliformisamine C
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Synthesis and Biological Investigation of Natural Product-Inspired Antimicrobial Compounds
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Fibrinogen and Clotting Characterization in COVID-19 Patients
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Synthetic Investigations into Small Molecules with Antibacterial Potential
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Site-Selective and Enantioselective C-H Functionalization of Unactivated C–H Bonds in the Presence of Nitrogen Functionality
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Synthesis of Novel EP2 Prostaglandin Antagonists for Optimal Blood-Brain Barrier Permeation as Radioligands
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Computational Development of Macrocyclic Drug Hits and Synthetic Strategy towards Peptide Macrocyclization
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A Tale of Two Chemistries: Dynamics of Delay-Coupled Belousov-Zhabotinsky Oscillators; TrkB Activators: A Review; Synthesis of TrkB Agonists
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Optimization of Rh2(S-TPPTTL)4 Through Ligand Diversification
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Unusual Paradigms in Selective Synthesis: Part 1: Toward the Synthesis of Racemic and Enantioenriched HIOC; Part 2: Fluorinated Alcohols: Powerful Promoters for the Ring-Opening Reactions of Epoxides with Carbon Nucleophiles
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Computational and Experimental Studies of Selective Rhodium-Catalyzed Allylic C–H Functionalization through π-Allyl Intermediates and Computational Development of Macrocycle Leads for Undruggable Targets
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