Journal ArticleDOI
The Photochemical and Thermal Interconversion of Some Cyclopentadienone Dimers
TLDR
In this paper, thermal and photochemical interconversions of isomeric diketones by skeletal rearrangements have been established to the extent summarized in schemes 2 and 3, and the intramolecular cycloaddition was found to be reversible photochemically.Abstract:
In continuation of previous work on cyclopentadienone dimers [3], thermal and photochemical interconversions of the isomeric diketones 1, 3, and 5 by skeletal rearrangements have been established to the extent summarized in schemes 2 and 3, and the intramolecular [2+2] cycloaddition 1 2 was found to be reversible photochemically.read more
Citations
More filters
Journal ArticleDOI
The [4 + 4] cycloaddition and its strategic application in natural product synthesis
Journal ArticleDOI
Synthese von Pentafulvalen durch oxidative Kupplung von Cyclopentadienid mittels Kupfer(II)-chlorid
TL;DR: In this article, a simple general synthetic concept for fulvalenes is outlined, consisting in an oxidative coupling of "Huckel anions" like 2 and 7 to 1, 1′-dihydrofulvalenes 10 with Ag(I) or Cu(II) salts, followed by deprotonation and oxidation.
Journal ArticleDOI
Radical cations of cyclopentadiene dimers—facets of an intriguing energy surface
TL;DR: The radical cations of various cyclopentadiene dimers can be generated by photoinduced electron transfer to strong electron acceptors as discussed by the authors, and nuclear spin polarization effects observed during these reactions provide insight into the radical cation structures.
Journal ArticleDOI
Photochemische Umlagerungen und Fragmentierungen von Alkenen und Polyenen
Journal ArticleDOI
Fulven‐Dimere: Synthese, Strukturbeweis and thermisches Verhalten
TL;DR: Fulvene-Dieters: Synthesis, Structure Elucidation and Thermal Behaviour as discussed by the authors, gives oligomeric mixtures consisting mainly of the endo-[4 + 2]-eycloaddition products 2a, 2b and 2c.
References
More filters
Journal ArticleDOI
Mechaisms of Photochemical Reactions in Solution. XXVIII.1 Values of Triplet Excitation energies of Selected Sensitizers
Related Papers (5)
Heterodiamantane und strukturell verwandte Verbindungen II. Pentacyclische Diäther der C10‐Reihe: 5,12‐Dioxapentacyclo‐[6.4.0.02,6.04,9]dodecan und 4,12‐Dioxapentacyclo[6.3.1.02,7.03,10.05,9]‐ dodecan
Nucleophilic Additions to Unactivated Carbon‐Carbon Double Bonds. Base‐Catalysed Ether Formation. Preliminary Communication
Willi Ammann,Camille Ganter +1 more