Lysergol monohydrate

In the title compound [systematic name: (7-methyl-4,6,6a,7,8,9-hexa­hydro­indolo[4,3,2-fg]quinoline-9-yl)methanol monohydrate], C(16)H(18)N(2)O·H(2)O, the non-aromatic ring (ring C of the ergoline skeleton) directly fused to the aromatic rings is nearly planar, with a maximum deviation of 0.659 (3) ...

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Detalles Bibliográficos
Autores principales: Merkel, Stefan, Köppen, Robert, Koch, Matthias, Emmerling, Franziska, Nehls, Irene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275264/
https://www.ncbi.nlm.nih.gov/pubmed/22347120
http://dx.doi.org/10.1107/S1600536812002632
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author Merkel, Stefan
Köppen, Robert
Koch, Matthias
Emmerling, Franziska
Nehls, Irene
author_facet Merkel, Stefan
Köppen, Robert
Koch, Matthias
Emmerling, Franziska
Nehls, Irene
author_sort Merkel, Stefan
collection PubMed
description In the title compound [systematic name: (7-methyl-4,6,6a,7,8,9-hexa­hydro­indolo[4,3,2-fg]quinoline-9-yl)methanol monohydrate], C(16)H(18)N(2)O·H(2)O, the non-aromatic ring (ring C of the ergoline skeleton) directly fused to the aromatic rings is nearly planar, with a maximum deviation of 0.659 (3) Å, and shows an envelope conformation. In the crystal, hydrogen bonds between the lysergol and water mol­ecules contribute to the formation of layers parallel to (10[Image: see text]).
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spelling pubmed-32752642012-02-15 Lysergol monohydrate Merkel, Stefan Köppen, Robert Koch, Matthias Emmerling, Franziska Nehls, Irene Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound [systematic name: (7-methyl-4,6,6a,7,8,9-hexa­hydro­indolo[4,3,2-fg]quinoline-9-yl)methanol monohydrate], C(16)H(18)N(2)O·H(2)O, the non-aromatic ring (ring C of the ergoline skeleton) directly fused to the aromatic rings is nearly planar, with a maximum deviation of 0.659 (3) Å, and shows an envelope conformation. In the crystal, hydrogen bonds between the lysergol and water mol­ecules contribute to the formation of layers parallel to (10[Image: see text]). International Union of Crystallography 2012-01-25 /pmc/articles/PMC3275264/ /pubmed/22347120 http://dx.doi.org/10.1107/S1600536812002632 Text en © Merkel et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Merkel, Stefan
Köppen, Robert
Koch, Matthias
Emmerling, Franziska
Nehls, Irene
Lysergol monohydrate
title Lysergol monohydrate
title_full Lysergol monohydrate
title_fullStr Lysergol monohydrate
title_full_unstemmed Lysergol monohydrate
title_short Lysergol monohydrate
title_sort lysergol monohydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275264/
https://www.ncbi.nlm.nih.gov/pubmed/22347120
http://dx.doi.org/10.1107/S1600536812002632
work_keys_str_mv AT merkelstefan lysergolmonohydrate
AT koppenrobert lysergolmonohydrate
AT kochmatthias lysergolmonohydrate
AT emmerlingfranziska lysergolmonohydrate
AT nehlsirene lysergolmonohydrate

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