Graphene oxide as a green carbon material for cross-coupling of indoles with ethers via oxidation and the Friedel–Crafts reaction

文献情報

出版日 2019-09-10

DOI 10.1039/C9QO00926D

インパクトファクター 5.281

著者

Yong Zen, Qian Liu, Hengshan Wang

原文を見る

要旨

Mild reaction conditions were developed to access 3,3′-bisindolylmethane derivatives with excellent regioselectivity at 25 °C based on a new graphene oxide (GO)-promoted alkylation strategy. To the best of our knowledge, these results constitute the first example of using a GO-based material as a carbon material to facilitate C(sp2)–C(sp3) bond formation.

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

Graphene oxide as a green carbon material for cross-coupling of indoles with ethers via oxidation and the Friedel–Crafts reaction

文献情報

おすすめジャーナル

関連文献

Facile protocol for the highly regioselective and stereodivergent synthesis of substituted bishomoallylic alcohols from esters

Direct intramolecular arylation of unactivated arenes: application to the synthesis of aporphine alkaloids

Selective growth of a less stable polymorph of 2-iodo-4-nitroaniline on a self-assembled monolayer template

Construction of a protein array on amyloid-like fibrils using co-assembly of designed peptides

Coordination polymers based on square planar Co(ii) node and linear spacer: solvent-dependent pseudo-polymorphism and an unprecedented interpenetrating structure containing both 2D and 3D topological isomers

Back matter

Chiral self-dimerization of vanadium complexes on a SiO2 surface: the first heterogeneous catalyst for asymmetric 2-naphthol coupling

Ni(iii) vs. Ni(ii)-thiyl radical: charge-delocalisation in a binuclear Ni(iii)Ni(ii)-dithiolate complex

Excimer formation by interstrand stacked pyrenes

Crystalline oligopyrene nanowires with multicolored emission

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

2-Nitrobenzotrifluoride

4-Hydroxy-2-(methylthio)pyrimidine-5-carbonitrile

2-Ethylhexyl dihydrogen phosphate

4-Bromoheptane

Tetrahydro-2H-pyran

おすすめサプライヤー