Potassium salt promoted regioselective three-component coupling synthesis of 1,4-asymmetrical [60]fullerene bisadducts with superior electron transport properties-Reference-Cited by-同舟云学术

Potassium salt promoted regioselective three-component coupling synthesis of 1,4-asymmetrical [60]fullerene bisadducts with superior electron transport properties

Published:2020 Issue:66 Volume:56 Page:9513-9516
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Li Fei¹²³⁴⁵^ORCID,Shang Yanbo⁶⁷⁸⁹¹⁰,Niu Chuang¹¹⁰¹¹⁵^ORCID,Li Chao¹²³⁴⁵,Huang Xinmin¹²³⁴⁵,Xu Guoyong¹²³⁴⁵,Xuan Jun¹²³⁴⁵,Zhou Hongping¹²³⁴⁵^ORCID,Yang Shangfeng⁶⁷⁸⁹¹⁰^ORCID

Affiliation:

1. Department of Chemistry

2. Key Laboratory of Functional Inorganic Materials of Anhui Province

3. Anhui University

4. Hefei 230039

5. China

6. Hefei National Laboratory for Physical Sciences at Microscale

7. Key Laboratory of Materials for Energy Conversion

8. Chinese Academy of Sciences

9. Department of Materials Science and Engineering

10. University of Science and Technology of China (USTC)

11. Hefei 230026

Abstract

An efficient one-pot three-component domino coupling reaction of phenols, C₆₀, and bromoalkanes was developed, resulting in the highly regioselective synthesis of 1,4-asymmetrical C₆₀ bisadducts.

Funder

National Natural Science Foundation of China

Anhui Department of Education

Natural Science Foundation of Anhui Province

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/CC/D0CC03857A

Reference59 articles.

1. A. Hirsch and M.Brettreich , Fullerenes: chemistry and reactions , Wiley-VCH Verlag GmbH & Co. KGaA , Weinheim , 2005

2. Functionalized Fullerenes in Water. The First 10 Years of Their Chemistry, Biology, and Nanoscience

3. New challenges in fullerene chemistry

4. Fullerene Polymers: Synthesis and Properties

5. Fullerene for organic electronics

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Synthesis of Diverse 1,4‐(Azaindole)[60]fullerenes via Transition‐Metal Free Three‐Component Coupling Reaction of Azaindoles, C₆₀, and Bromoalkanes/Triphenylamines^†;Chinese Journal of Chemistry;2023-08-17

2. One‐Pot Synthesis of Diverse 1,4‐[60]Fullerephenols via Three‐Component Umpolung Cascade Coupling of Phenols, C₆₀, and Nucleophiles;Chemistry – A European Journal;2023-05-08

3. Synthesis of diverse unsymmetric 1,4-adducts via a three-component coupling reaction of malonate derivatives, [60]fullerene and electrophiles/nucleophiles;Organic Chemistry Frontiers;2023

4. KO^tBu-Promoted, Three-Component Domino Reaction of Arenes(indoles/phenols), C₆₀, and (Per/poly)fluoroarenes: Achieving Direct C–C Cross-Coupling of Fullerene with (Per/poly)fluoroarenes;The Journal of Organic Chemistry;2022-12-20

5. Transition-Metal-Free Domino Reaction of [60]Fullerene, Indole, and DMSO/HCl: One-Pot Access to Diverse N-Substituted [60]Fulleroindole Derivatives;The Journal of Organic Chemistry;2022-06-07