A versatile strategy for difunctionalization of carbon–carbon multiple bonds by photoredox catalysis

文献情報

出版日 2016-05-31

DOI 10.1039/C6QO00139D

インパクトファクター 5.281

著者

Takashi Koike, Munetaka Akita

原文を見る

要旨

Photoredox catalysis has emerged as a strong synthetic tool for radical reactions. In particular, a variety of regioselective difunctionalizations of carbon–carbon multiple bonds through SET photoredox processes (oxidative quenching cycle) have been accomplished by an appropriate choice of an electrophilic radical precursor and a nucleophile. The basic concept, representative results and future prospect are the topics of this article.

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

A versatile strategy for difunctionalization of carbon–carbon multiple bonds by photoredox catalysis

文献情報

おすすめジャーナル

関連文献

Self-assembly of a bis(adeninyl)–Cu(i) complex: a cationic nucleobase duplex mimic

Back matter

Molecular beacon-functionalized gold nanoparticles as probes in dry-reagent strip biosensor for DNA analysis

Room-temperature aerobic formation of a stable aryl–Cu(iii) complex and its reactions with nucleophiles: highly efficient and diverse arene C–H functionalizations of azacalix[1]arene[3]pyridine

Colorimetric and fluorometric detection of cationic surfactants based on conjugated polydiacetylene supramolecules

G-quadruplex-based DNAzyme for sensitive mercury detection with the naked eye

Back matter

Monodisperse Pt and PtRu/C60 hybrid nanoparticles for fuel cell anode catalysts

Spiropyran-linked dipeptide forms supramolecular hydrogel with dual responses to light and to ligand–receptor interaction

Magnetic PEDOT hollow capsules with single holes

こちらもおすすめ

3-(5-フェニル-2-ファイル)-プロパン酸の市場動向や研究トレンドはどうですか？

3- Chloro-1H-indazol-5-olはどのように保存すればよいですか？

二茂鐵是安全的吗？

L-(1-~13~C)メチオニンの市場動向や研究トレンドはどうですか？

1,3-フェニレンビスメチレンビスアクリレートは安全ですか？

丹参醇Aはどのように保存すればよいですか？

4-メチル-2-(1,1,1-三フロロ-2-メチルプロパニル)ピリドインとは何ですか？

N-フェニルベンジル-2-クロロ酢氨を取り扱う際の実験室安全事項は何ですか？

UCN-02を取り扱う際の実験室安全事項は何ですか？

N-[3-[2-(二甲基氨基)乙氧基]-4-甲氧基苯基]-2'-甲基-4'-(5-甲基-1,2,4-恶二唑-3-基)-[1,1'-联苯]-4-甲酰胺を取り扱う際の実験室安全事項は何ですか？

掲載誌

Organic Chemistry Frontiers

おすすめ化合物

6,7-Dimethoxy-4(1H)-quinolinone

N,N'-1,2-Ethanediylbis(N-acetylacetamide)

4-Chloro-2,3-dimethylpyridine 1-oxide

Narcissin

Diethyl 1,1-cyclopropanedicarboxylate

おすすめサプライヤー