Imino Diels-Alder adducts. XII. Two pyrano[3,2-c]quinolines

The crystal structures of pyrano­quinolines 9‐fluoro‐5‐phenyl‐3,4,4a,5,6,10b‐hexa­hydro‐2H‐pyrano[3,2‐c]quinoline, C18H18FNO, and 9‐methyl‐5‐phenyl‐3,4,4a,5,6,10b‐hexa­hydro‐2H‐pyrano­[3,2‐c]quinoline, C19H21NO, are isomorphous. In both structures, the pyran ring is exo to the six‐membered N‐heteroc...

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Veröffentlicht in:Acta crystallographica. Section C, Crystal structure communications Crystal structure communications, 2006-09, Vol.62 (9), p.o574-o576
Hauptverfasser: Ravikumar, K., Sridhar, B., Mahesh, M., Reddy, V. V. Narayana
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Sprache:eng
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Zusammenfassung:The crystal structures of pyrano­quinolines 9‐fluoro‐5‐phenyl‐3,4,4a,5,6,10b‐hexa­hydro‐2H‐pyrano[3,2‐c]quinoline, C18H18FNO, and 9‐methyl‐5‐phenyl‐3,4,4a,5,6,10b‐hexa­hydro‐2H‐pyrano­[3,2‐c]quinoline, C19H21NO, are isomorphous. In both structures, the pyran ring is exo to the six‐membered N‐heterocyclic ring formed in the cyclo­addition step. The torsion angles across the phenyl linkage for the two structures are −91.2 (1) and −88.3 (2)°. The striking feature in both crystal packings is that they do not contain the expected conventional hydrogen bonds, in spite of the presence of good hydrogen‐bonding functionalities. Possible C—H⋯π inter­actions are, however, observed.
ISSN:0108-2701
1600-5759
DOI:10.1107/S0108270106029465