Nicht-äquilibrierende Diradikale: Stereochemie der thermischen Reorganisation methylsubstituierter 6-Methylen-bicyclo[3.2.0]hept-2-ene
- 1 April 1975
- journal article
- zuschrift
- Published by Wiley in Angewandte Chemie
- Vol. 87 (7) , 252-254
- https://doi.org/10.1002/ange.19750870717
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- Hydrocarbon thermal degenerate rearrangements. VI. Boat Cope transition state in self-interconversion of 1,4-dimethylenecyclohexaneJournal of the American Chemical Society, 1974
- [1,3]-Sigmatropic rearrangement with retention of configuration forced upon the migrating groupJournal of the American Chemical Society, 1974
- Stereochemie der entarteten Norcaradien‐Umlagerung: Ein stereospezifischer orbitalsymmetrie‐verbotener ProzeßAngewandte Chemie, 1974
- Stereochemistry of the Degenerate Norcaradiene Rearrangement: A Stereospecific Symmetry‐Forbidden ProcessAngewandte Chemie International Edition in English, 1974
- Continuous diradical as transition state. Internal rotational preference in the thermal enantiomerization and diastereoisomerization of cis- and trans-1-cyano-2-isopropenylcyclopropaneJournal of the American Chemical Society, 1974
- Rotationsbarriere in 1,2‐Dienen; Resonanzenergie des Allyl‐RadikalsEuropean Journal of Inorganic Chemistry, 1974
- Subjacent orbital control. Electronic factor favoring concertedness in Woodward-Hoffmann forbidden reactionsJournal of the American Chemical Society, 1972
- Aromaticity and Pericyclic ReactionsAngewandte Chemie International Edition in English, 1971
- Aromatizität und pericyclische ReaktionenAngewandte Chemie, 1971
- Steric prohibition of the inversion pathway. Test of the orbital symmetry prediction of the sense of rotation in thermal suprafacial 1,3-sigmatropic rearrangementsJournal of the American Chemical Society, 1970