Ru(ii)-Catalyzed C7-acyloxylation of indolines with carboxylic acids

文献情報

出版日 2018-07-30

DOI 10.1039/C8OB01603H

インパクトファクター 3.876

著者

Pinaki Bhusan De, Sonbidya Banerjee, Sourav Pradhan, Tharmalingam Punniyamurthy

原文を見る

要旨

Ruthenium(II)-catalyzed site-selective C7-acyloxylation of indolines with carboxylic acids is presented. The substrate scope and functional group tolerance are important practical features. The kinetic isotope studies suggest that C–H bond activation may be the rate-determining step.

掲載誌

Organic & Biomolecular Chemistry

CiteScore: 3.4

自己引用率: 10.3%

年間論文数: 1041

Organic & Biomolecular Chemistry (OBC) publishes original and high impact research and reviews in organic chemistry. We welcome research that shows new or significantly improved protocols or methodologies in total synthesis, synthetic methodology or physical and theoretical organic chemistry as well as research that shows a significant advance in the organic chemistry or molecular design aspects of chemical biology, catalysis, supramolecular and macromolecular chemistry, theoretical chemistry, mechanism-oriented physical organic chemistry, medicinal chemistry or natural products. Articles published in the journal should report new work which makes a highly-significant impact in the field. Routine and incremental work is generally not suitable for publication in the journal. More details about key areas of our scope are below. In all cases authors should include in their article clear rationale for why their research has been carried out.

Ru(ii)-Catalyzed C7-acyloxylation of indolines with carboxylic acids

文献情報

おすすめジャーナル

関連文献

Inside back cover

Fine structure in the solution state 13C-NMR spectrum of C60 and its endofullerene derivatives

The eternal battle to combat global warming: (thio)urea as a CO2 wet scrubbing agent

Surface-orientation- and ligand-dependent quenching of the spin magnetic moment of Co porphyrins adsorbed on Cu substrates

Site dependent reactivity of Pt single atoms on anatase TiO2(101) in an aqueous environment

Nonadiabatic sunlight harvesting

Fragment-based quantum mechanical approach to biomolecules, molecular clusters, molecular crystals and liquids

Inside back cover

Density-functional theory models of Fe(iv)O reactivity in metal–organic frameworks: self-interaction error, spin delocalisation and the role of hybrid exchange

Structural characterization of molybdenum–dinitrogen complex as key species toward ammonia formation by dispersive XAFS spectroscopy

こちらもおすすめ

除水剤ALT-201は安全ですか？

「邻羟基阿托伐他汀内酯标准品」に適用される法規ガイドelinesは何ですか？

メチル（3R）-3-アミノ-2,3-ジヒドロ-1-ベンゾファンラニン-5-カルボイル酸塩塩酸塩の主な用途は何ですか？

トランス-4-メチルピロリジン-3-オール塩酸塩はどのように合成されますか？

硫雜環丁烷-1,1-二氧化物は安全ですか？

ブラエリリンの主な用途は何ですか？

9-ヒドロキシエリプチシネ塩酸塩はどのように合成されますか？

5-塩素-2-(メチルアミノ)フェニル-(2-塩素フェニル)メタン酮の物理化学的性質は何ですか？

1-[2-(4-甲氧基-苯氧基)-乙基]-哌嗪はどのように保存すればよいですか？

2-[3-(4-甲氧基フェニル)プロピル]-4,4,5,5-四メチル-1,3,2-ドイボロロールアンの主な用途は何ですか？

掲載誌

Organic & Biomolecular Chemistry

おすすめ化合物

N,4-Dimethylaniline hydrochloride (1:1)

1-Chloro-2-(chlorophenylmethyl)benzene

2-Sulfanyl-3-pentanone

1,3(2H,4H)-Isoquinolinedione, 7-amino-4,4-dimethyl-

6-Iodo-1,2-benzothiazol-3(2H)-one 1,1-dioxide

おすすめサプライヤー