1,2,3- versus 1,2-Indeno Ring Fusions Influence Structure Property and Chirality of Corannulene Bowls-Reference-Cited by-同舟云学术

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1,2,3- versus 1,2-Indeno Ring Fusions Influence Structure Property and Chirality of Corannulene Bowls

Published:2018-03-26 Issue:7 Volume:83 Page:3979-3986
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Shi¹,Roch Loïc M.¹²,Allemann Oliver¹²,Xu Jun¹,Vanthuyne Nicolas³,Baldridge Kim K.¹^ORCID,Siegel Jay S.¹

Affiliation:

1. Health Science Platform, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, PR China

2. Department of Chemistry, University of Zurich, Winterthurerstrasse 190, 8057 Zurich, Switzerland

3. Aix Marseille Univ, CNRS, Centrale Marseille, iSm2, Marseille, France

Funder

Ministry of Science and Technology of the People's Republic of China

Synergetic Innovation Center of Chemical Science and Engineering, Tianjin University

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.8b00320

Reference50 articles.

1. Synthesis, Structures, and Physical Properties of Aromatic Molecular-Bowl Hydrocarbons

2. Structure/Energy Correlation of Bowl Depth and Inversion Barrier in Corannulene Derivatives: Combined Experimental and Quantum Mechanical Analysis

3. Pentaindenocorannulene and Tetraindenocorannulene: New Aromatic Hydrocarbon π Systems with Curvatures Surpassing That of C60

4. Aromatic π-Systems More Curved Than C60. The Complete Family of All Indenocorannulenes Synthesized by Iterative Microwave-Assisted Intramolecular Arylations

5. Synthesis of Fluoranthenes and Indenocorannulenes: Elucidation of Chiral Stereoisomers on the Basis of Static Molecular Bowls

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