Journal of Medicinal Chemistry p. 2671 - 2677 (1991)
Update date:2022-08-02
Topics:
Davey
Erhardt
Cantor
Greenberg
Ingebretsen
Wiggins
A series of novel imidazoquinoxalinones and their aza analogues were prepared by the cyclization of o-amino(1H-imidazol-1-yl)aryls and heteroaryls with carbonyldiimidazole. The compounds were screened for inhibition of Type I and Type IV phosphodiesterase
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