Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

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Nitrosation of aryl and heteroaryltrifluoroborates with nitrosonium tetrafluoroborate

P2860

Q42149283-8CE5E4D4-5ABE-42DA-AC27-A6F263F1D172

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Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

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2010 nî lūn-bûn

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2010年の論文

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年学术文章

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2010年學術文章

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Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

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Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

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type

Item

label

Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

@en

Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

@nl

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Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

@en

Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

@nl

P1476

Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

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P2093

Hironao Sajiki

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

Shigeki Mori

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

Tomohiro Maegawa

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

Toshihide Maejima

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

Yasunari Monguchi

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P2860

Azides: their preparation and synthetic uses

Biaryl Phosphane Ligands in Palladium-Catalyzed Amination

Palladium-catalyzed coupling of ammonia with aryl chlorides, bromides, iodides, and sulfonates: a general method for the preparation of primary arylamines.

Organic azides: an exploding diversity of a unique class of compounds.

Preparation of potassium azidoaryltrifluoroborates and their cross-coupling with aryl halides.

Synthesis of aryl azides and vinyl azides via proline-promoted CuI-catalyzed coupling reactions.

CuI/4-hydro-L-proline as a more effective catalytic system for coupling of aryl bromides with N-boc hydrazine and aqueous ammonia.

A very simple copper-catalyzed synthesis of anilines by employing aqueous ammonia.

Ammonium salts as an inexpensive and convenient nitrogen source in the Cu-catalyzed amination of aryl halides at room temperature.

Ligand-free Sonogashira coupling reactions with heterogeneous Pd/C as the catalyst.

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7372-7375

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scholarly article

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10.1002/CHEM.200903511

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

P407

English

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

P478

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

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2010-07-01T00:00:00Z

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

P698

20486103

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Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

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P2860

P2860

Copper-mediated reductive amination of aryl halides with trimethylsilyl azide.

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type

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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