Synthesis of Diverse 1,4‐(Azaindole)[60]fullerenes via <scp>Transition‐Metal</scp> Free <scp>Three‐Component</scp> Coupling Reaction of Azaindoles, <scp>C<sub>60</sub></scp>, and Bromoalkanes/Triphenylamines<sup>†</sup>-Reference-Cited by-同舟云学术

Synthesis of Diverse 1,4‐(Azaindole)[60]fullerenes via Transition‐Metal Free Three‐Component Coupling Reaction of Azaindoles, C₆₀, and Bromoalkanes/Triphenylamines^†

Published:2023-08-17 Issue:22 Volume:41 Page:2975-2980
ISSN:1001-604X
Container-title:Chinese Journal of Chemistry
language:en
Short-container-title:Chin. J. Chem.

Author:

Huang Xinmin¹²,Liu Zi‐Zheng¹,Cheng Jia‐Qi¹,Cao Cheng‐Yu¹,Li Peng‐Cheng¹,Xuan Jun¹,Li Fei¹²

Affiliation:

1. Department of Chemistry, Anhui University; Key Laboratory of Structure and Functional Regulation of Hybrid Materials (Anhui University), Ministry of Education; Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials and Key Laboratory of Functional Inorganic Materials of Anhui Province Hefei Anhui 230601 China

2. Department of Chemistry University of Science and Technology of China Hefei Anhui 230026 China

Abstract

Comprehensive SummaryA transition‐metal free three‐component coupling reaction of azaindoles, C60, and bromoalkanes/triphenylamines has been developed to provide an efficient access to diverse azaindole functionalized 1,4‐C60 adducts. This protocol exhibits low cost, operational simplicity, wide substrate scope, and mild and convenient conditions.

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cjoc.202300292

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