Electrochemically Enabled, Nickel-Catalyzed Amination.

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Electrifying Organic Synthesis.Ni-Catalyzed Electrochemical Decarboxylative C-C Couplings in Batch and Continuous Flow.Electrochemical synthesis of AuPt nanoflowers in deep eutectic solvent at low temperature and their application in organic electro-oxidation

P2860

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P2860

Electrochemically Enabled, Nickel-Catalyzed Amination.

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http://www.wikidata.org/entity/Q48188882

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2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

@zh

2017年學術文章

@zh-hant

name

Electrochemically Enabled, Nickel-Catalyzed Amination.

@en

Electrochemically Enabled, Nickel-Catalyzed Amination.

@nl

type

Item

label

Electrochemically Enabled, Nickel-Catalyzed Amination.

@en

Electrochemically Enabled, Nickel-Catalyzed Amination.

@nl

prefLabel

Electrochemically Enabled, Nickel-Catalyzed Amination.

@en

Electrochemically Enabled, Nickel-Catalyzed Amination.

@nl

P1476

Electrochemically Enabled, Nickel-Catalyzed Amination

@en

P2093

Chao Li

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

Denghui Bao

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

Jeremy T Starr

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

Jinshan Chen

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

Ming Yan

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

Qinglong Hou

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

Yu Kawamata

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

Zhiqing Liu

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

P2860

Synthetic Organic Electrochemistry: An Enabling and Innately Sustainable Method

The application of cathodic reductions and anodic oxidations in the synthesis of complex molecules

Nickel-Catalyzed Amination of Aryl Chlorides and Sulfamates in 2-Methyl-THF

Development of an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates

Induced protein degradation: an emerging drug discovery paradigm.

Palladium-Catalyzed Coupling of Functionalized Primary and Secondary Amines with Aryl and Heteroaryl Halides: Two Ligands Suffice in Most Cases

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

Structural basis of PROTAC cooperative recognition for selective protein degradation

Challenging nickel-catalysed amine arylations enabled by tailored ancillary ligand design.

Aryl amination using ligand-free Ni(II) salts and photoredox catalysis.

P304

13088-13093

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P31

scholarly article

P356

10.1002/ANIE.201707906

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P407

English

P433

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

P478

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

P50

Phil S Baran

Hugh Nakamura

Julien C Vantourout

P577

2017-09-14T00:00:00Z

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P698

28834098

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P921

Iztāctepoztli

P932

5792186

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

Electrochemically Enabled, Nickel-Catalyzed Amination.

about

P2860

P2860

Electrochemically Enabled, Nickel-Catalyzed Amination.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P698

P921

P932