Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

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Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

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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

Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

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Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

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type

Item

label

Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

@en

Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

@nl

prefLabel

Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

@en

Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

@nl

P1476

Copper-catalyzed ipso-selenation of aromatic carboxylic acids.

@en

P2093

Ge Wu

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

Hongchen Li

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

Huayue Wu

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

Jinchang Ding

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

Jing Wang

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

Miaochang Liu

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

Tao Leng

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

Wenxia Gao

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

Xiaobo Huang

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P2860

Synthesis of biaryls via catalytic decarboxylative coupling

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Chemistry of biologically important synthetic organoselenium compounds.

Decarboxylative coupling reactions: a modern strategy for C-C-bond formation.

Selenium- and tellurium-containing fluorescent molecular probes for the detection of biologically important analytes.

3-(3,4,5-Trimethoxyphenylselenyl)-1H-indoles and their selenoxides as combretastatin A-4 analogs: microwave-assisted synthesis and biological evaluation.

Metal-Catalyzed Decarboxylative C-H Functionalization.

Asymmetric, organocatalytic, three-step synthesis of alpha-hydroxy-(E)-beta,gamma-unsaturated esters.

Unexpected C-Se cross-coupling reaction: copper oxide catalyzed synthesis of symmetrical diaryl selenides via cascade reaction of selenourea with aryl halides/boronic acids.

P304

9718-9726

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P31

scholarly article

P356

10.1039/C7OB02066J

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P433

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

P478

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

P577

2017-11-01T00:00:00Z

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P698

29165471

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