作者: Masahiko Kato , Masaru Mitsuda , Tomoko Tatsumoto , Rika Uchida , Akio Ichimura
DOI: 10.1246/CL.1989.1789
关键词:
摘要: Benzo[1,2:4,5]dicycloheptene-3,6,9,12-tetraone was synthesized in two different routes. Its 1st and 2nd redox potentials (E1 = −0.14 V, E2 −0.74 V) were found to be more positive than those of 7H-benzocycloheptene-1,4,7-trione −0.31 −0.90 under the same conditions.