C–H activation-enabled synthesis of a piperazine-embedded azadibenzo[<i>a</i>,<i>g</i>]corannulene analogue-Reference-Cited by-同舟云学术

C–H activation-enabled synthesis of a piperazine-embedded azadibenzo[a,g]corannulene analogue

Published:2024 Issue:10 Volume:11 Page:2807-2814
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Huang Lin¹²³,Qiu Mengyu¹²³,Chang Zhihao¹²³,Browne Duncan L.⁴^ORCID,Huang Jianhui¹²³^ORCID

Affiliation:

1. School of Pharmaceutical Science and Technology (SPST), Faculty of Medicine, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, P. R. China

2. International Joint Research Centre for Molecular Sciences, Tianjin University, Tianjin 300072, China

3. Innovation Center of Chemical Science and Engineering, Tianjin 300072, China

4. Department of Pharmaceutical and Biological Chemistry, University College London (UCL), School of Pharmacy, 29-39 Brunswick Square, Bloomsbury, London, WC1N 1AX, UK

Abstract

The first example of an azadibenzo[a,g]corannulene analogue with an embedded piperazine ring on the flank of its polycyclic skeleton is reported.

Funder

National Basic Research Program of China

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/QO/D4QO00415A

Reference62 articles.

1. The crystal and molecular structure of corannulene, C20H10

2. Multiethynyl Corannulenes: Synthesis, Structure, and Properties

3. Enantiopure C 5 Pentaindenocorannulenes: Chiral Graphenoid Materials

4. Diazapentabenzocorannulenium: A Hydrophilic/Biophilic Cationic Buckybowl

5. Synthesis and dynamics of the corannulene nucleus

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