1,3-Dipolar cycloaddition of polycyclic azomethine ylide to norcorroles: towards dibenzoullazine-fused derivatives-Reference-Cited by-同舟云学术

1,3-Dipolar cycloaddition of polycyclic azomethine ylide to norcorroles: towards dibenzoullazine-fused derivatives

Published:2022 Issue:45 Volume:58 Page:6510-6513
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Li Sha¹,Sun Yahan¹,Li Xiaofang¹,Smaga Oskar²^ORCID,Koniarz Sebastian²^ORCID,Stępień Marcin²^ORCID,Chmielewski Piotr J.²^ORCID

Affiliation:

1. Key Laboratory of Theoretical Organic Chemistry and Functional Molecules, Ministry of Education, School of Chemistry and Chemical Engineering, Hunan University of Science and Technology Xiangtan, Hunan 411201, China

2. Department of Chemistry, University of Wrocław, F. Joliot-Curie 14, 50 383 Wrocław, Poland

Abstract

Reaction of polycyclic azomethine ylide with norcorrole resulted in a family of chiral antiaromatic stereoisomeric cycloadducts. Oxidative dehydrogenation of some of them gave rise to the dibenzoullazine-extended norcorroles.

Funder

National Natural Science Foundation of China

Narodowe Centrum Nauki

Science and Technology Program of Hunan 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/2022/CC/D2CC02071H

Reference48 articles.

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2. Aromatic and antiaromatic ring currents in a molecular nanoring

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5. Integrated Materials Design of Organic Semiconductors for Field-Effect Transistors

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