A very large quinone was prepared by the double Diels-Alder reaction of 2,5
,9,12-tetra(t-butyl)diacenaphtho[1,2-b: 1',2'-d]thiophene and benzoquinone.
The crystal structure of the polycyclic product shows that the central ant
hraquinone ring system is quite twisted (50 degrees), and the overall struc
ture possesses approximate D-2 symmetry. (C) 2000 Elsevier Science Ltd. All
rights reserved.