83320-84-7Relevant articles and documents
Azulenes by Vacuum Pyrolysis of Halotricyclo4,6>decadienes
Dehmlow, Eckehard V.,Balschukat, Dietmar
, p. 3805 - 3816 (2007/10/02)
Double addition of halocarbenes or -carbenoids to cyclooctatetraene yields the title compounds 2.Pyrolysis of these (700 deg C, 0.01 mbar) gives azulenes of varying substitution patterns (4, 5, 6, and/or 7) which carry one substituent in each ring.Structure assignments follow from 1H NMR spectroscopy, sometimes after electrophilic introduction of the trifluoroacetyl residue.Nucleophilic substitutions of azulenes with two halogen atoms (giving compounds 8 or 9) occur only in the 7-membered ring; only 4b and CuCN yield some 11 in addition to 10.
9-PHENYLBICYCLONONATETRAENYL ANION A NEW DIATROPIC 10 ?-ELECTRON SYSTEM
Kawase, Takeshi,Oda, Masaji
, p. 2677 - 2678 (2007/10/02)
Treatment of 9-chloro-9-phenylbicyclonona-2,4,6-triene with excess bases gives, by the intermediacy of 9-phenylbicyclo-1(9),2,4,6-tetraene, 9-phenylbicyclotetraenyl anion of which (1)H-NMR spectrum suggests some diatropic character of