Substituenteneinflüsse auf das Valenzgleichgewicht 4,8‐substituierter Homotropilidene
Author:
Affiliation:
1. Fachbereich Chemie der Universität Kaiserslautern, Postfach 3049, D‐6750 Kaiserslautern
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19841170213
Reference39 articles.
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4. A rapidly reversible degenerate cope rearrangement
5. 1,3,5,7-Tetramethylbicyclo[5.1.0]octa-2,5-diene (tetramethylhomotropilidene) by a 1,4-homoelimination reaction. Stereochemical analysis of a Cope rearrangement
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2. Preparation of gem-dimethylcyclopropane-fused compounds through sigmatropic rearrangements. On/off-switching of the tautomerization of 3,4-homotropilidene by steric hindrance;Tetrahedron;2002-11
3. The Cycloaddition-Cycloelimination Pathway to Homotropilidenes − Synthesis and Properties of Homotropilidenes;European Journal of Organic Chemistry;2001-07
4. Enantiospecific preparation of gem-dimethylcyclopropane fused cycloheptanes via valence tautomerization of 3,4-homotropilidene under thermodynamic and kinetic control;Tetrahedron Letters;1996-09
5. Substituent effects on the geometries and energies of cyclopropanes and the corresponding 2-propyl derivatives;Journal of the American Chemical Society;1984-08
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