Hydrogen bonding in two tetracyclic indole alkaloids

dc.contributor.author Varma, Ashok K.
dc.contributor.author Nangia, Ashwini
dc.contributor.author Desiraju, Gautam R.
dc.contributor.author Giri, Venkatachalam S.
dc.contributor.author Jaisankar, Parasuraman
dc.date.accessioned 2022-03-27T09:32:57Z
dc.date.available 2022-03-27T09:32:57Z
dc.date.issued 2001-01-01
dc.description.abstract 3-Acetyl-1,6,7,12b-tetrahydroindolo[2,3-a]quinolizin-2(12H)-one, C17H16N2O2, consists of two symmetry-independent molecules and each forms a layered structure stabilized by N-H···O and C-H···O hydrogen bonds. In 3-acetyl-6,7-dihydroindolo[2,3-a]quinolizin-4(12H)-one monohydrate, C17H14N2O2·H2O, the structure is stabilized by O-H···O, N-H···O and C-H···O hydrogen bonds, with the ordered water molecule playing a crucial role in the self-assembly. Contribution from the weak interactions to the strong hydrogen-bonded network is a common feature in both structures.
dc.identifier.citation Acta Crystallographica, Section C: Crystal Structure Communications. v.57(1)
dc.identifier.issn 01082701
dc.identifier.uri 10.1107/S0108270100014220
dc.identifier.uri http://scripts.iucr.org/cgi-bin/paper?S0108270100014220
dc.identifier.uri https://dspace.uohyd.ac.in/handle/1/13039
dc.title Hydrogen bonding in two tetracyclic indole alkaloids
dc.type Journal. Article
dspace.entity.type
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