Manganese catalyzed N-alkylation of anilines with alcohols: ligand enabled selectivity

文献情報

出版日 2018-10-08

DOI 10.1039/C8OB01886C

インパクトファクター 3.876

著者

Vinod G. Landge, Akash Mondal, Vinit Kumar, Avanashiappn Nandakumar, Ekambaram Balaraman

原文を見る

要旨

Ligand enabled Earth-abundant manganese catalyzed N-alkylation of amines with alcohols via a hydrogen auto-transfer strategy is reported. The choice of the ligand plays a significant role in the alcohol reactivity (aliphatic or aromatic) toward N-alkylation reactions.

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.

Manganese catalyzed N-alkylation of anilines with alcohols: ligand enabled selectivity

文献情報

おすすめジャーナル

関連文献

Transitioning organic synthesis from organic solvents to water. What's your E Factor?

Low melting mixtures based on β-cyclodextrin derivatives and N,N′-dimethylurea as solvents for sustainable catalytic processes

Hydrogenation of levulinic acid to γ-valerolactone by Ni and MoOx co-loaded carbon catalysts

Highly active, water-compatible and easily separable magnetic mesoporous Lewis acid catalyst for the Mukaiyama–Aldol reaction in water

An efficient and stable star-shaped plasticizer for starch: cyclic phosphazene with hydrogen bonding aminoethoxy ethanol side chains

A nickel doped perovskite catalyst for reforming methane rich biogas with minimal carbon deposition

A survey of solvent selection guides

Catalytic bio–chemo and bio–bio tandem oxidation reactions for amide and carboxylic acid synthesis

Harvest of Cu NP anchored magnetic carbon materials from Fe/Cu preloaded biomass: their pyrolysis, characterization, and catalytic activity on aqueous reduction of 4-nitrophenol

Magnetic gold nanocatalyst (nanocat-Fe–Au): catalytic applications for the oxidative esterification and hydrogen transfer reactions

こちらもおすすめ

6-苄基-6,7-二氢-5H-吡咯并3,4-b吡啶とは何ですか？

半硫酸奎宁单水水合物はどのように保存すればよいですか？

D-核糖-5-リン酸二ナトリウムとは何ですか？

異丙基肼はどの業界で使用されていますか？

3-乙酰基-4-羟基喹啉-2(1H)-酮はどのように合成されますか？

Bobcat339はどのように保存すればよいですか？

5-溴-4-甲基-1H-吲唑とは何ですか？

3-(4メトキシフェニル)オキテナン-3カーボイル酸の代替品はありますか？

3-イリドオキシピロロ[2,3-b]ピリジン-5-カルボキシlic酸は安全ですか？

3-氟-4- iodobenolを取り扱う際の実験室安全事項は何ですか？

掲載誌

Organic & Biomolecular Chemistry

おすすめ化合物

5-(4-Fluorophenyl)-1,3,4-oxadiazol-2(3H)-one

1,4-Dioxecane-5,10-dione

(3R,4aR,7aS,9aR,10S,11R,13aR,13bS,15aS,15bR)-3,11-Dihydroxy-10-(hydroxymethyl)-4,4,7a,10,13a,15b-hexamethyl-1,2,3,4,4a,7,7a,8,9,9a,10,11,12,13,13a,13b,14,15,15a,15b-icosahydro-5H-naphtho[2',1':4,5]cyc lohepta[1,2-a]naphthalen-5-one

Tribromoerbium hydrate (1:1)

8-Fluoroquinolin-3-ylboronic acid

おすすめサプライヤー