The Peculiar Behavior of Electronically Excited Cyclobutanones: A Photochemical Example of the Consequence of Through-Bond Interaction
Author:
Publisher
Wiley
Subject
General Chemistry,Catalysis
Reference10 articles.
1. Tieftemperatur-elektronenspektroskopische Beobachtungen zur lichtinduzierten Cyclobutanon/Tetrahydrofuryliden-Umlagerung
2. For previous examples of the chemical consequences of through-bond coupling, see: and Spec. Lect. XXIIIrd Int. Congr. Pure Appl. Chem., Vol. 1, p. 157, Butterworths, London 1971.
3. Stereospezifität als Argument gegen die Intermediärrolle von 1,4-Alkyl/Acyl-Diradikalen bei der lichtinduzierten Cyclobutanon/Tetrahydrofuryliden-Isomerisierung in kondensierter Phase
4. Stereospecificity as an Argument against the Intermediacy of 1,4-Alkyl/Acyl Diradicals in the Light-Induced Cyclobutanone-Tetrahydrofurylidene Isomerization in Condensed Phase
5. Interaction of orbitals through space and through bonds
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1. Photochemical reaction mechanism of cyclobutanone: CASSCF study;International Journal of Quantum Chemistry;2003-10-02
2. Homolysis of Carbenes. Free Radicals from Dialkoxycarbenes;Journal of the American Chemical Society;1998-10-16
3. Photocycloeliminations of bicyclic cyclobutanones I-solvent effects on distribution of products;Structural Chemistry;1991-02
4. Photochemical, photophysical, and theoretical studies on cyclobutanethiones. .alpha.-Cleavage reactions;The Journal of Organic Chemistry;1988-02
5. Molecular orbital calculations of excited state cyclobutanone and its photocarbene;Tetrahedron;1988-01
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