Is Kekulene Really Superaromatic?
- 1 November 1996
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 35 (20) , 2383-2386
- https://doi.org/10.1002/anie.199623831
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- [5]Pericyclynes Are Not HomoaromaticThe Journal of Organic Chemistry, 1996
- Aromaticity and Antiaromaticity in Five‐Membered C4H4X Ring Systems: “Classical” and “Magnetic” Concepts May Not Be “Orthogonal”Angewandte Chemie International Edition in English, 1995
- Aromatizität und Antiaromatizität in fünfgliedrigen C4H4X‐Ringsystemen: beschreibbar durch „klassische”︁ und „magnetische”︁ KonzepteAngewandte Chemie, 1995
- Are kekulene, coronene, and corannulene tetraanion superaromatic? Theoretical examination using hardness indicesJournal of Physical Organic Chemistry, 1995
- Non-superaromatic reference defined by graph theory for a super-ring moleculeJournal of the Chemical Society, Faraday Transactions, 1995
- Is superaromaticity a fact or an artifact? The kekulene problemJournal of the American Chemical Society, 1992
- Localization of aromaticity in fused-ring cycloarene systems. Prediction by an effective molecular mechanics modelThe Journal of Organic Chemistry, 1988
- Structures and 1H‐chemical shifts of conjugation deficient hydrocarbonsInternational Journal of Quantum Chemistry, 1986
- Benzoide versus annulenoide Aromatizität: Synthese und Eigenschaften des KekulensAngewandte Chemie, 1978
- On the Number of Aromatic Sextets in a Benzenoid HydrocarbonBulletin of the Chemical Society of Japan, 1976