Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose? - Test2 - elhamkhani - TriplyDB

Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose?

Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose?

http://www.wikidata.org/entity/Q28066537

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Ring-Expansion Approach to Medium-Sized Lactams and Analysis of Their Medicinal Lead-Like Properties.Lewis Acid Induced Toggle from Ir(II) to Ir(IV) Pathways in Photocatalytic Reactions: Synthesis of Thiomorpholines and Thiazepanes from Aldehydes and SLAP Reagents.Bioactive Natural Product and Superacid Chemistry for Lead Compound Identification: A Case Study of Selective hCA III and L-Type Ca2+ Current Inhibitors for Hypotensive Agent Discovery.Divergent Synthesis of Cyclopropane-Containing Lead-Like Compounds, Fragments and Building Blocks through a Cobalt Catalyzed Cyclopropanation of Phenyl Vinyl Sulfide Synthesis of Spirocyclic Pyrrolidines: Advanced Building Blocks for Drug Discovery.Modular synthesis of thirty lead-like scaffolds suitable for CNS drug discovery.

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Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose?

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2016 nî lūn-bûn

@nan

2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2016 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2016年の論文

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2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

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2016年论文

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Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose?

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Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose?

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Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose?

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Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose?

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Evaluating New Chemistry to Drive Molecular Discovery: Fit for Purpose?

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Stephen P. Marsden

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KNIME-CDK: Workflow-driven cheminformatics

Defining desirable central nervous system drug space through the alignment of molecular properties, in vitro ADME, and safety attributes

From Heteroaromatic Acids and Imines to Azaspirocycles: Stereoselective Synthesis and 3D Shape Analysis

Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings

Silylation of C–H bonds in aromatic heterocycles by an Earth-abundant metal catalyst

A divergent synthetic approach to diverse molecular scaffolds: assessment of lead-likeness using LLAMA, an open-access computational tool.

Factors determining the selection of organic reactions by medicinal chemists and the use of these reactions in arrays (small focused libraries).

Medicinal chemical properties of successful central nervous system drugs

Enumeration of 166 billion organic small molecules in the chemical universe database GDB-17.

Synthesis and profiling of a diverse collection of azetidine-based scaffolds for the development of CNS-focused lead-like libraries.

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13650-13657

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10.1002/ANIE.201604193

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Stephen P. Marsden

Daniel J. Foley

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