Facile Friedel–Crafts alkylation of arenes under solvent-free conditions-Reference-Cited by-同舟云学术

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Facile Friedel–Crafts alkylation of arenes under solvent-free conditions

Published:2024 Issue:11 Volume:22 Page:2187-2191
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Chen Feijing¹,Zhao Xiao-Xiao¹,Zhang Hao-Tian¹,Ma Yan-Na¹^ORCID,Chen Xuenian¹^ORCID

Affiliation:

1. College of Chemistry, Zhengzhou University, Zhengzhou, 450001, Henan, China

Abstract

Herein, we developed an efficient HOTf-promoted Friedel–Crafts alkylation reaction of broad arenes with α-aryl-α-diazoesters under metal-free and solvent-free conditions.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Henan Province

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D4OB00162A

Reference73 articles.

1. Catalytic Asymmetric Arylation of α-Aryl-α-diazoacetates with Aniline Derivatives

2. Chiral 1,1-diaryl compounds as important pharmacophores

3. Influence of the oxidative stress induced by the organophosphate pesticide bromopropylate on the mitochondrial respiratory chain in Trichoderma harzianum

4. Palladium-Catalyzed α-Arylation of Esters

5. Palladium/Copper-Catalyzed Di-α-arylation of Acetic Acid Esters

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