Cyclic allenes or diradicals in the cyclization reactions of dienynes generated by photolysis of alkynylcyclohexadienones

Citation
M. Fernandez-zertuche et al., Cyclic allenes or diradicals in the cyclization reactions of dienynes generated by photolysis of alkynylcyclohexadienones, J ORG CHEM, 65(17), 2000, pp. 5207-5211
Citations number
21
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
JOURNAL OF ORGANIC CHEMISTRY
ISSN journal
00223263 → ACNP
Volume
65
Issue
17
Year of publication
2000
Pages
5207 - 5211
Database
ISI
SICI code
0022-3263(20000825)65:17<5207:CAODIT>2.0.ZU;2-Y
Abstract
Reported here are some rearrangements involving the electrocyclic ring clos ure of dieneynes 7. Such ring closures are envisaged to possibly give strai ned substituted cyclic allenes 8 which could also behave as diradicals 8a. The results show that compounds such as 5 rearrange to cyclohexadienones 9a , 9b, or 11 through these kind of intermediates. Theoretical calculations p erformed on simple models similar to the intermediates suggest that the nat ure of these intermediates correspond to that of cyclic allenes.