Exocyclic Charge Flight from Cyclopropenide Systems as a Criterion of Antiaromaticity
- 1 January 1980
- journal article
- research article
- Published by Wiley in Israel Journal of Chemistry
- Vol. 20 (3-4) , 319-320
- https://doi.org/10.1002/ijch.198000091
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- Bond fixation in annulenes. 6. Equalization of ring inversion and bond shifting energetics in methyl-substituted cyclooctatetraenes. Use of buttressing effects for comparing transition-state geometriesJournal of the American Chemical Society, 1979
- Is antiaromaticity absolute?Journal of the American Chemical Society, 1978
- Conjugative Stabilization in an “Antiaromatic” System: The Conformational Mobility of 1,5‐Bisdehydro[12]annuleneHelvetica Chimica Acta, 1977
- 1,3(Nonbonded) carbon/carbon interactions. The common cause of ring strain, puckering, and inward methylene rocking in cyclobutane and of vertical nonclassical stabilization, pyramidalization, puckering, and outward methylene rocking in the cyclobutyl cationJournal of the American Chemical Society, 1977