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In the mol­ecule of 4-(2-chloro­phenyl)­pyrrolo­[1,2-a]­quinoxa­line, C17H11ClN2, (I), the bond lengths are consistent with electron delocalization in the two outer rings of the fused tricyclic system, with a localized double bond in the central ring. The mol­ecules of (I) are linked into chains by a [pi]-[pi] stacking inter­action. In (4RS)-4-(1,3-benzo­dioxol-6-yl)-4,5-di­­hydro­pyrrolo­[1,2-a]­quinoxaline, C18H14N2O2, (II), the central ring of the fused tricyclic system adopts a conformation inter­mediate between screw-boat and half-chair forms. A combination of N-H...O and C-H...[pi](arene) hydrogen bonds links the mol­ecules of (II) into a sheet. Comparisons are made with related compounds.
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