Cu-catalyzed C–N bond cleavage of 3-aminoindazoles for the C–H arylation of enamines

文献情報

出版日 2019-11-01

DOI 10.1039/C9QO01177C

インパクトファクター 5.281

著者

Yao Zhou, Ya Wang, Zhiyi Song, Tamaki Nakano

原文を見る

要旨

The Cu-catalyzed C–H arylation of enamines via the oxidative C–N cleavage of 3-aminoindazoles is presented. A diverse array of arylated enamines were produced in decent yields with a wide substrate scope under mild conditions. Here, 3-aminoindazoles were harnessed as novel arylating agents via a radical process.

掲載誌

Organic Chemistry Frontiers

CiteScore: 7.8

自己引用率: 8.7%

年間論文数: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Cu-catalyzed C–N bond cleavage of 3-aminoindazoles for the C–H arylation of enamines

文献情報

おすすめジャーナル

関連文献

Phase-transfer alkylation reactions using microreactors

A two-step field-induced magnetic transition in a novel layered cobalt diphosphonate

Phosphinine stabilised gold nanoparticles; synthesis and immobilisation on mesoporous materials

A novel migrative addition reaction of hydrazines to the diketone derivative of C60

Synthesis of monodisperse chromium nanoparticles from the thermolysis of a Fischer carbene complex

Highly substituted pyridinesvia tethered imine–enamine (TIE) methodology

Enzymatic preparation of biotinylated naturally-occurring sialylglycan and its molecular recognition on a quartz-crystal microbalance

Iron(iii) salen-type catalysts for the cross-coupling of aryl Grignards with alkyl halides bearing β-hydrogens

A new type of bromide anion conducting solid

Palladium catalysed cyclisation–carbonylation of enynes to give cyclic γ,δ-unsaturated acids

こちらもおすすめ

環戊烷-1,3-二甲酸甲酯はどのように合成されますか？

4-メトキシ-1,2,3-スチアゼ-3,5-ジオンとは何ですか？

プロスタグランジンA2について「に適用される法規ガイドラインは何ですか？'

4-アミノ-1-ナフタレン sulfonic 酸についての物理化学的性質は何ですか？

N-GlcNAc-生物素を取り扱う際の実験室安全事項は何ですか？

3-アミノメチルフローラノピペリジン-1-カルボニル酸テルブチルエステルとは何ですか？

6-溴-1-甲基-1H-ベンゾ[d][1,2,3]三氮唑はどのように合成されますか？

4-硫代尿苷はどのように合成されますか？

ブレインナトリユリックペプチド32ラットとは何ですか？

1-(3-氮杂啶)-4-羟基哌啶双盐酸盐の物理化学的性質は何ですか？

掲載誌

Organic Chemistry Frontiers

おすすめ化合物

Magnesium taurate

2,5-Dichloro-3-methylthiophene

Ethyl 4-cyanobenzoate

Diisopropylphosphoramidous dichloride

Ethyl (R)-(-)-mandelate

おすすめサプライヤー