Iptycenes with an acridinone motif developed through [4+2] cycloaddition of tethered naphthalene and iminoquinone via a radical reaction-Reference-Cited by-同舟云学术

Iptycenes with an acridinone motif developed through [4+2] cycloaddition of tethered naphthalene and iminoquinone via a radical reaction

Published:2017 Issue:46 Volume:53 Page:6247-6250
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Raju Selvam¹²³⁴^ORCID,Annamalai Pratheepkumar¹²³⁴^ORCID,Chen Pei-Ling⁵⁶³⁷,Liu Yi-Hung⁸⁹¹⁰⁴,Chuang Shih-Ching¹²³⁴^ORCID

Affiliation:

1. Department of Applied Chemistry

2. National Chiao Tung University

3. Hsinchu

4. Taiwan 30010

5. Department of Chemistry

6. National Tsing Hua University

7. Taiwan 30013

8. Instrumentation Center

9. National Taiwan University

10. Taipei

Abstract

A new class of iptycenes was developed by combining 2-(naphthalen-1-yl)anilines and p-benzoquinones through copper(ii)-mediated radical cyclisation.

Funder

Ministry of Science and Technology, Taiwan

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/2017/CC/C7CC03030D

Reference33 articles.

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3. S. Diez-Gonzalez , N-Heterocyclic Carbenes, Royal Society of Chemistry, 2010

4. Pentiptycene-based concave NHC–metal complexes

5. Iptycenes in supramolecular and materials chemistry

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