Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids. - Wikidata - awgldk - TriplyDB

Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.

Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.

http://www.wikidata.org/entity/Q41828474

about

Radicals: Reactive Intermediates with Translational Potential Redox-Active Esters in Fe-Catalyzed C-C Coupling.Beyond ferryl-mediated hydroxylation: 40 years of the rebound mechanism and C-H activation.Ni-Catalyzed C-C Couplings Using Alkyl Electrophiles.Cross-coupling of aromatic esters and amides.Selective uni- and bidirectional homologation of diborylmethane.Highly nucleophilic vitamin B12-assisted nickel-catalysed reductive coupling of aryl halides and non-activated alkyl tosylates.Alkyl-(Hetero)Aryl Bond Formation via Decarboxylative Cross-Coupling: A Systematic Analysis.A Dual Palladium and Copper Hydride Catalyzed Approach for Alkyl-Aryl Cross-Coupling of Aryl Halides and Olefins.Nickel-Catalyzed Barton Decarboxylation and Giese Reactions: A Practical Take on Classic Transforms.Alkyl Esterification of Vinylarenes Enabled by Visible-Light-Induced Decarboxylation.Decarboxylative Alkynylation.Decarboxylative borylation.Reductive Decarboxylative Alkynylation of N-Hydroxyphthalimide Esters with Bromoalkynes.Harnessing Alkyl Amines as Electrophiles for Nickel-Catalyzed Cross Couplings via C-N Bond Activation.Nickel-Catalyzed Heck-Type Monofluoroacetation of Styrenes for Facile Synthesis of Allylic Fluorides.Nickel-catalyzed acetamidation and lactamization of arylboronic acids.Nickel-Catalyzed Enantioselective Cross-Coupling of N-Hydroxyphthalimide Esters with Vinyl Bromides.Ni-Catalyzed Electrochemical Decarboxylative C-C Couplings in Batch and Continuous Flow.CITU: A Peptide and Decarboxylative Coupling Reagent.Base-free nickel-catalysed decarbonylative Suzuki-Miyaura coupling of acid fluorides Building C(sp)-rich complexity by combining cycloaddition and C-C cross-coupling reactions Kupferkatalysierte decarboxylierende radikalische Silylierung von redoxaktiven aliphatischen Carbonsäurederivaten

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P2860

Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.

http://www.wikidata.org/entity/Q41828474

description

2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.

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type

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Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.

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Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids.

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Angewandte Chemie International Edition

P1476

Nickel-Catalyzed Cross-Coupling of Redox-Active Esters with Boronic Acids

@en

P2093

Benjamin Vokits

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

Jacob T Edwards

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Jie Wang

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Laurin Wimmer

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

Scott A Shaw

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

Tian Qin

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

Tie-Gen Chen

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P2860

A general alkyl-alkyl cross-coupling enabled by redox-active esters and alkylzinc reagents

Big Data from Pharmaceutical Patents: A Computational Analysis of Medicinal Chemists' Bread and Butter.

Asymmetric Suzuki cross-couplings of activated secondary alkyl electrophiles: arylations of racemic alpha-chloroamides

Dual catalysis. Merging photoredox with nickel catalysis: coupling of α-carboxyl sp³-carbons with aryl halides.

Practical Ni-Catalyzed Aryl-Alkyl Cross-Coupling of Secondary Redox-Active Esters.

Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: The missing link.

Nickel-catalyzed Negishi arylations of propargylic bromides: a mechanistic investigation

Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners

Analysis of Past and Present Synthetic Methodologies on Medicinal Chemistry: Where Have All the New Reactions Gone?

New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles.

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9676-9679

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scholarly article

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10.1002/ANIE.201605463

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33

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55

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27380912

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5232357

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