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> Abstr Conf Comb Chem Jpn
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Abstr Conf Comb Chem Jpn
14th
Discovery of Biomimetic Asymmetric Catalysts Using Fluorescence-Based Screens.
14th Conference on Combinatorial Chemistry, Japan: Solid-Phase Synthesis of Benzopyran Libraries for Combinatorial Chemistry via Highly Efficient Hydroxyl-alkoxylation.
High Throughput Drug Discovery.
High Throughput Purification with On-line Characterization.
Bridging Hit to Lead: Application of Pharmacophore Models in Scaffold Design.
Combining in silico and ex silico Approaches in Combinatorial Library Design.
Synthesis and Biological Evaluation of a Targeted Library of Curacin A Analogs.
Sulfone-based Linkers in Solid-phase Organic Synthesis: Sulfone and Sulfinate Chemistry.
Focused Substance Libraries for Lead Optimisation.
Application of Microwave Dielcric Heating for Rapid Reaction Optimisations and Liberary Synthesis.
Combinatorial Catalysis Discovery: Highly Active and Air-Stable Palladium Catalysts for Cross-Coupling Reactions of Aryl Chlorides.
Integrated Material Chip Technology for Speeding up Solid State Materials Research.
New phase tagging strategies for high throughput solution phase synthesis.
New Methods for High-Throughput Organic Synthesis.
Design and Synthesis of Nano-Devices Using Functional DNAs Obtained by Combinatorial Chemistry.
Toward Proteomimetics: .ALPHA.-Helical Peptide Libraries on a Phage surface.
15th
Dynamic Asymmetric Activation: Super High-Throughput Screening of Chiral Ligands and Activators by HPLC-CD/UV and HPLC-OR/RIU.
Hit to Lead and Lead to Candidate Optimisation using Multi-parametric Principles.
Applications of Sequential Multi-Component Reactions to Focused Libraries.
Chemical library approaches to target validation in the post-genomic era.
Improving Purity of Parallel Synthesis Products.
Peptide Microarrays using Structure-based Libraries for Protein Detection.
Interfacing Natural Product and Combinatorial Chemistry in the Discovery of New Antibiotics.
Developing Superior Human Therapeutics: Exploiting Novel Chemical Genomics Strategies in Drug Discovery.
Comparative Study of Synthesis Surfaces Support Matrices for Library Generation.
Transition-Metal-Based Lewis Acid- and Base-Catalyzed Multicomponent Reactions directed toward Combinatorial Chemistry.
Discovery of a Novel M3 Receptor Selective Antagonist by Combinatorial Chemistry Approach.
Structural Development of Retinoids and Thalidomide.
Recent Trends of Micro Flow Devices and Systems for Chemical/Biochemical Applications.
Extending the boundary of Automation: A solution phase synthesizer for medicinal and process chemists.
Development of A Parallel Synthetic Approach To Ether-Linked Phospholipids Using a Parallel Synthesizer.
Evolution in the Test Tube as a Means to Create Enantioselective Enzymes.
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