Verbesserte Synthese von 2,6-Dicyan-1,5-dimethylsemibullvalen aus 1,5-Dimethylbicyclo[3.3.0]octan-3,7-dion
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Reference81 articles.
1. Die Ergebnisse sind Teil der Dissertation von Univ. Würzburg 1988.
2. Temperaturabhängigkeit des UV-Spektrums von 1,5-Dimethyl-2,6-semibullvalendicarbonitril, Hinweis auf ein Gleichgewicht mit einem delokalisierten, homoaromatischen Isomer
3. Temperature Dependence of the UV Spectrum of 1,5-Dimethyl-2,6-semibullvalenedicarbonitrile; Evidence for an Equilibrium with a Delocalized, Homoaromatic Isomer
4. Ph. D. Thesis, City University of New York 1982;
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1. Experimental and Theoretical Study of Stabilization of Delocalized Forms of Semibullvalenes and Barbaralanes by Dipolar and Polarizable Solvents. Observation of a Delocalized Structure that Is Lower in Free Energy than the Localized Form;The Journal of Organic Chemistry;2005-03-29
2. Lifting of the Degeneracy in Semibullvalenes by Remote and Direct Substituents: A Quantitative Study Using Variable-Temperature Carbon-13 NMR Spectroscopy;The Journal of Organic Chemistry;2001-02-20
3. Semibullvalenes—Homoaromatic bovines?;Advances in Theoretically Interesting Molecules;1998
4. Design of substituted semibullvalenes suitable for control of the cope rearrangement by two ps IR laser pulses;Chemical Physics;1995-07
5. 2,6‐Dimethyl Semibullvalene‐2,6‐dicarboxylates;Chemische Berichte;1992-11
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