An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe(CN)6].

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Mild palladium-catalyzed cyanation of (hetero)aryl halides and triflates in aqueous media.Ex situ generation of stoichiometric HCN and its application in the Pd-catalysed cyanation of aryl bromides: evidence for a transmetallation step between two oxidative addition Pd-complexes.

P2860

Q34992489-BA28F7BA-0372-410D-BAF4-0CD8DEB8F60A Q52345388-D4143687-888E-4EBF-95B4-D3EE34048EE4

P2860

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe(CN)6].

Item

http://www.wikidata.org/entity/Q50503075

description

2012 nî lūn-bûn

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2012年の論文

@ja

2012年学术文章

@wuu

2012年学术文章

@zh

2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

@zh-hant

name

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe

@nl

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe(CN)6].

@en

type

Item

label

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe

@nl

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe(CN)6].

@en

prefLabel

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe

@nl

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe(CN)6].

@en

P1476

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe(CN)6].

@en

P2093

Chunpu Li

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

Dengyou Zhang

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

Haifeng Sun

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

Hong Liu

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

Hualiang Jiang

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

Kaixian Chen

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

Lei Zhang

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

Yu Zhou

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

P2860

Recent developments and perspectives in palladium-catalyzed cyanation of aryl halides: synthesis of benzonitriles.

Acridone-based inhibitors of inosine 5'-monophosphate dehydrogenase: discovery and SAR leading to the identification of N-(2-(6-(4-ethylpiperazin-1-yl)pyridin-3-yl)propan-2-yl)-2- fluoro-9-oxo-9,10-dihydroacridine-3-carboxamide (BMS-566419).

Increasing rates and scope of reactions: sluggish amines in microwave-heated aminocarbonylation reactions under air.

Phenethylthiazolylthiourea (PETT) compounds as a new class of HIV-1 reverse transcriptase inhibitors. 2. Synthesis and further structure-activity relationship studies of PETT analogs.

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

Azaindoles: moderately basic P1 groups for enhancing the selectivity of thrombin inhibitors.

Rapid, easy cyanation of aryl bromides and chlorides using nickel salts in conjunction with microwave promotion.

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.

Palladium-Catalyzed Cyanation of Aryl Halides: Recent Developments and Perspectives

P304

2909-2911

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P31

scholarly article

P356

10.1039/C2CC17468E

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P407

English

P433

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

P478

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

P577

2012-02-03T00:00:00Z

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

P698

22307456

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

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe(CN)6].

about

P2860

P2860

An expedient Pd/DBU mediated cyanation of aryl/heteroaryl bromides with K4[Fe(CN)6].

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P577

P698