90522-51-3Relevant academic research and scientific papers
Oxyanion-assisted Retro-Diels-Alder Reactions in the Tricyclo2,8>nona-3,6-diene (Barbaralane) System
Miyashi, Tsutomu,Ahmed, Alauddin,Mukai, Toshio
, p. 179 - 180 (1984)
9-Vinyl- and 9-aryl-tricyclo2,8>nona-3,6-dien-9-olates (1c - h) underwent the retro-Diels-Alder reaction to give cycloheptatrienes (2c - h) in excellent yields, indicating that it is not necessary for the fragmented 4? component to be incorporated into an aromatic nucleus.
Light-Sensitive Dihydroazulenes: Alternative Synthesis - The Influence of Alkyl Substituents at the Five-Memeered Ring on the Photochromic Behaviour
Gierisch, Sebastian,Daub, Joerg
, p. 69 - 76 (2007/10/02)
Starting from cycloheptatrienylium tetrafluoroborate (8) the dihydroazulenes 1 were synthesized via substituted cycloheptatrienes 10 - 13 as intermediates.The dicyanovinyl derivatives 12 and 13 were transformed into vinylheptafulvenes 2 by dehydrogenation
