Correction: Palladium-catalyzed oxidative annulation of in situ generated enones to pyrroles: a concise route to functionalized indoles

文献情報

出版日 2016-01-12

DOI 10.1039/C6QO90004F

インパクトファクター 5.281

著者

Tenglong Guo, Quanbin Jiang

原文を見る

要旨

Correction for ‘Palladium-catalyzed oxidative annulation of in situ generated enones to pyrroles: a concise route to functionalized indoles’ by Tenglong Guo et al., Org. Chem. Front., 2015, 2, 1361–1365.

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

Correction: Palladium-catalyzed oxidative annulation of in situ generated enones to pyrroles: a concise route to functionalized indoles

文献情報

おすすめジャーナル

関連文献

Diels–Alder crosslinked HA/PEG hydrogels with high elasticity and fatigue resistance for cell encapsulation and articular cartilage tissue repair

Cyclodextrin–calixarene co-polymers as a new class of nanosponges

Contents list

Solution-dispersed porous hyperbranched conjugated polymer nanoparticles for fluorescent sensing of TNT with enhanced sensitivity

Reactive macromolecular micelle crosslinked highly elastic hydrogel with water-triggered shape-memory behaviour

Front cover

Polythiol copolymers with precise architectures: a platform for functional materials

Mesogen-jacketed liquid crystalline polymers with peripheral oligo(ethylene oxide) chains: phase structure and thermoresponsive behavior

Low band-gap copolymers derived from fluorinated isoindigo and dithienosilole: synthesis, properties and photovoltaic applications

Synthesis of core cross-linked star polystyrene with functional end groups and self-assemblies templated by breath figures

こちらもおすすめ

1-{3-[5-(エチルカルボンイル)-2,4-ジメチル-1H-ピロロール-3-基]プロパニル}ピペリジン-4-カルボン酸について、適用される法規ガイドラインは何ですか？

2,2-二氟-1,3-ベンゾジオキサン-5-カルボキシlic酸とは何ですか？

8-氯-4-色原酮の代替品はありますか？

エチル6,6-ジメチル-4,5,6,7-テトラヒドロ-1H-インドアゼー-3-カルボキシレートとは何ですか？

4-叔丁基-6-氯-嘧啶に適用される法規ガイドラインは何ですか？

維库溴铵杂质Bはどのように合成されますか？

2-(4-氟苄基)-吡咯烷の物理化学的性質は何ですか？

3-喹啉甲醛（2-チロール-8-エチル）は安全ですか？

エチル3-(ヒドロキシメチル)-1H-ピロール-2-カルボキシレートはどのように保存すればよいですか？

哌拉西林杂质Dは安全ですか？

掲載誌

Organic Chemistry Frontiers

おすすめ化合物

Ethyl 4-oxo-1-piperidinecarboxylate

Tris(2-ethylhexyl) 4,4',4''-(1,3,5-triazine-2,4,6-triyltriimino)tribenzoate

Glycol salicylate

Butylphenyl Methylpropional

2,6-Dibromopyridine

おすすめサプライヤー