Glycozolidal

The title compound known as glycozolidal (systematic name: 2,7-dimeth­oxy-9H-carbazole-3-carbaldehyde), C(15)H(13)NO(3), is a naturally occurring carbazole, which was isolated from the roots of Clausena lansium. The carbazole ring system is essentially planar, with an r.m.s. deviation of 0.0093 (1) ...

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Autores principales: Fun, Hoong-Kun, Maneerat, Wisanu, Laphookhieo, Surat, Chantrapromma, Suchada
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151865/
https://www.ncbi.nlm.nih.gov/pubmed/21837182
http://dx.doi.org/10.1107/S1600536811024160
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author Fun, Hoong-Kun
Maneerat, Wisanu
Laphookhieo, Surat
Chantrapromma, Suchada
author_facet Fun, Hoong-Kun
Maneerat, Wisanu
Laphookhieo, Surat
Chantrapromma, Suchada
author_sort Fun, Hoong-Kun
collection PubMed
description The title compound known as glycozolidal (systematic name: 2,7-dimeth­oxy-9H-carbazole-3-carbaldehyde), C(15)H(13)NO(3), is a naturally occurring carbazole, which was isolated from the roots of Clausena lansium. The carbazole ring system is essentially planar, with an r.m.s. deviation of 0.0093 (1) Å. In the crystal, inter­molecular N—H⋯O hydrogen bonds connect the mol­ecules into a chain along the c axis. C—H⋯O, C—H⋯π and π–π inter­actions, with centroid–centroid distances of 3.5924 (6), 3.6576 (6) and 3.8613 (6) Å, are also observed.
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spelling pubmed-31518652011-08-11 Glycozolidal Fun, Hoong-Kun Maneerat, Wisanu Laphookhieo, Surat Chantrapromma, Suchada Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound known as glycozolidal (systematic name: 2,7-dimeth­oxy-9H-carbazole-3-carbaldehyde), C(15)H(13)NO(3), is a naturally occurring carbazole, which was isolated from the roots of Clausena lansium. The carbazole ring system is essentially planar, with an r.m.s. deviation of 0.0093 (1) Å. In the crystal, inter­molecular N—H⋯O hydrogen bonds connect the mol­ecules into a chain along the c axis. C—H⋯O, C—H⋯π and π–π inter­actions, with centroid–centroid distances of 3.5924 (6), 3.6576 (6) and 3.8613 (6) Å, are also observed. International Union of Crystallography 2011-06-25 /pmc/articles/PMC3151865/ /pubmed/21837182 http://dx.doi.org/10.1107/S1600536811024160 Text en © Fun et al. 2011 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
Fun, Hoong-Kun
Maneerat, Wisanu
Laphookhieo, Surat
Chantrapromma, Suchada
Glycozolidal
title Glycozolidal
title_full Glycozolidal
title_fullStr Glycozolidal
title_full_unstemmed Glycozolidal
title_short Glycozolidal
title_sort glycozolidal
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151865/
https://www.ncbi.nlm.nih.gov/pubmed/21837182
http://dx.doi.org/10.1107/S1600536811024160
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AT chantraprommasuchada glycozolidal

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