Redox reaction between benzyl azides and aryl azides: concerted synthesis of aryl nitriles and anilines.

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Redox reaction between benzyl azides and aryl azides: concerted synthesis of aryl nitriles and anilines.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年学术文章

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2017年學術文章

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2017年學術文章

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name

Redox reaction between benzyl ...... of aryl nitriles and anilines.

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Redox reaction between benzyl ...... of aryl nitriles and anilines.

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Item

label

Redox reaction between benzyl ...... of aryl nitriles and anilines.

@en

Redox reaction between benzyl ...... of aryl nitriles and anilines.

@nl

prefLabel

Redox reaction between benzyl ...... of aryl nitriles and anilines.

@en

Redox reaction between benzyl ...... of aryl nitriles and anilines.

@nl

P1476

Redox reaction between benzyl ...... of aryl nitriles and anilines.

@en

P2093

Jaiwook Park

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

Yongjin Kim

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

Young Ho Rhee

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

P2860

A convenient new procedure for converting primary amides into nitriles.

Mild palladium-catalyzed cyanation of (hetero)aryl halides and triflates in aqueous media.

An efficient transformation from benzyl or allyl halides to aryl and alkenyl nitriles.

Copper-catalyzed domino halide exchange-cyanation of aryl bromides.

Aminocyclopentadienyl ruthenium complexes as racemization catalysts for dynamic kinetic resolution of secondary alcohols at ambient temperature.

Potassium hexacyanoferrate(II)--a new cyanating agent for the palladium-catalyzed cyanation of aryl halides.

Mild and efficient copper-catalyzed cyanation of aryl iodides and bromides.

Transnitrilation from Dimethylmalononitrile to Aryl Grignard and Lithium Reagents: A Practical Method for Aryl Nitrile Synthesis.

Aerobic Copper-Promoted Radical-Type Cleavage of Coordinated Cyanide Anion: Nitrogen Transfer to Aldehydes To Form Nitriles.

Green synthesis of nitriles using non-noble metal oxides-based nanocatalysts.

P304

1636-1641

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P31

scholarly article

P356

10.1039/C6OB02615J

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P433

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

P478

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

P577

2017-01-26T00:00:00Z

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P698

28124712

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