Stereospecificity as an Argument against the Intermediacy of 1,4‐Alkyl/Acyl Diradicals in the Light‐Induced Cyclobutanone‐Tetrahydrofurylidene Isomerization in Condensed Phase
- 1 March 1974
- journal article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 13 (3) , 197-198
- https://doi.org/10.1002/anie.197401971
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Photochemical ring expansion of cyclic aliphatic ketones. Cyclobutanones and cyclopentanonesJournal of the American Chemical Society, 1973
- Determination of the average singlet-triplet splitting in biradicals by measurement of the magnetic field dependence of CIDNP [chemically induced dynamic nuclear polarization]Journal of the American Chemical Society, 1973
- Chemically induced dynamic nuclear spin polarization derived from biradicals generated by photochemical cleavage of cyclic ketones, and the observation of a solvent effect on signal intensitiesJournal of the American Chemical Society, 1972
- Drei über verschiedene Zustände der Elektronenenergie führende Isomerisierungswege eines linear-konjugierten CyclohexadienonsAngewandte Chemie, 1972
- Interaction of orbitals through space and through bondsAccounts of Chemical Research, 1971
- Stereospecific photoreactions of cyclobutanonesJournal of the American Chemical Society, 1970
- Lichtinduzierte Säurebildung aus cyclischen KetonenAngewandte Chemie, 1965
- Light‐Induced Formation of Acids from Cyclic KetonesAngewandte Chemie International Edition in English, 1965