Trifluoroacetic acid in 2,2,2-trifluoroethanol facilitates S(N)Ar reactions of heterocycles with arylamines.

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Structure-guided design of purine-based probes for selective Nek2 inhibition Cyclin-Dependent Kinase (CDK) Inhibitors: Structure-Activity Relationships and Insights into the CDK-2 Selectivity of 6-Substituted 2-Arylaminopurines.

P2860

Q36189360-B8BFD0B9-8BB1-427B-A506-22631C4F60A1 Q48124327-2D7E39DC-588E-44FA-A84A-5A78E7F499B6

P2860

Trifluoroacetic acid in 2,2,2-trifluoroethanol facilitates S(N)Ar reactions of heterocycles with arylamines.

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http://www.wikidata.org/entity/Q46942024

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

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name

Trifluoroacetic acid in 2,2,2- ...... heterocycles with arylamines.

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Trifluoroacetic acid in 2,2,2- ...... heterocycles with arylamines.

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type

Item

label

Trifluoroacetic acid in 2,2,2- ...... heterocycles with arylamines.

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Trifluoroacetic acid in 2,2,2- ...... heterocycles with arylamines.

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Trifluoroacetic acid in 2,2,2- ...... heterocycles with arylamines.

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Trifluoroacetic acid in 2,2,2- ...... heterocycles with arylamines.

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P1476

Trifluoroacetic acid in 2,2,2- ...... f heterocycles with arylamines

@en

P2093

Amy R Roberts

http://www.w3.org/2001/XMLSchema#string

Benoit Carbain

http://www.w3.org/2001/XMLSchema#string

Bernard T Golding

http://www.w3.org/2001/XMLSchema#string

Celine Cano

http://www.w3.org/2001/XMLSchema#string

Christopher J Matheson

http://www.w3.org/2001/XMLSchema#string

Christopher R Coxon

http://www.w3.org/2001/XMLSchema#string

Christopher Wong

http://www.w3.org/2001/XMLSchema#string

David M Turner

http://www.w3.org/2001/XMLSchema#string

Honorine Lebraud

http://www.w3.org/2001/XMLSchema#string

Ian R Hardcastle

http://www.w3.org/2001/XMLSchema#string

P2860

Structure-based design of a potent purine-based cyclin-dependent kinase inhibitor

Biaryl Phosphane Ligands in Palladium-Catalyzed Amination

Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides

Diaryl- and triaryl-pyrrole derivatives: inhibitors of the MDM2-p53 and MDMX-p53 protein-protein interactions†Electronic supplementary information (ESI) available: Experimental details for compound synthesis, analytical data for all compounds and in

Kinase-likeness and kinase-privileged fragments: toward virtual polypharmacology.

Asymmetric catalysis of epoxide ring-opening reactions.

The medicinal chemist's toolbox: an analysis of reactions used in the pursuit of drug candidates.

Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide.

Controlled microwave heating in modern organic synthesis.

The element effect revisited: factors determining leaving group ability in activated nucleophilic aromatic substitution reactions.

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2311-2317

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scholarly article

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10.1002/CHEM.201304336

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English

P433

http://www.w3.org/2001/XMLSchema#string

P478

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Elisa Meschini

P577

2014-01-23T00:00:00Z

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24458729

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Trifluoroacetic acid in 2,2,2-trifluoroethanol facilitates S(N)Ar reactions of heterocycles with arylamines.

about

P2860

P2860

Trifluoroacetic acid in 2,2,2-trifluoroethanol facilitates S(N)Ar reactions of heterocycles with arylamines.

description

name

type

label

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P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698