Cargando…
N-Methyl-2-thiocytisine
The rings of the three-ring cytisine system in the title compound [systematic name: (1R,5S)-1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocine-8-thione], C(12)H(16)N(2)S, have planar [maximum deviation 0.0170 (7) Å], half-chair and chair conformations. In the crystal structure, relat...
Autores principales: | , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007573/ https://www.ncbi.nlm.nih.gov/pubmed/21588268 http://dx.doi.org/10.1107/S1600536810025870 |
_version_ | 1782194390205202432 |
---|---|
author | Owczarzak, Anita M. Przybył, Anna K. Kubicki, Maciej |
author_facet | Owczarzak, Anita M. Przybył, Anna K. Kubicki, Maciej |
author_sort | Owczarzak, Anita M. |
collection | PubMed |
description | The rings of the three-ring cytisine system in the title compound [systematic name: (1R,5S)-1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocine-8-thione], C(12)H(16)N(2)S, have planar [maximum deviation 0.0170 (7) Å], half-chair and chair conformations. In the crystal structure, relatively short and directional C—H⋯π interactions and weaker secondary C—H⋯S contacts join the molecules into helical chains along the [001] direction. |
format | Text |
id | pubmed-3007573 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30075732010-12-30 N-Methyl-2-thiocytisine Owczarzak, Anita M. Przybył, Anna K. Kubicki, Maciej Acta Crystallogr Sect E Struct Rep Online Organic Papers The rings of the three-ring cytisine system in the title compound [systematic name: (1R,5S)-1,2,3,4,5,6-hexahydro-1,5-methano-8H-pyrido[1,2-a][1,5]diazocine-8-thione], C(12)H(16)N(2)S, have planar [maximum deviation 0.0170 (7) Å], half-chair and chair conformations. In the crystal structure, relatively short and directional C—H⋯π interactions and weaker secondary C—H⋯S contacts join the molecules into helical chains along the [001] direction. International Union of Crystallography 2010-07-07 /pmc/articles/PMC3007573/ /pubmed/21588268 http://dx.doi.org/10.1107/S1600536810025870 Text en © Owczarzak et al. 2010 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 Owczarzak, Anita M. Przybył, Anna K. Kubicki, Maciej N-Methyl-2-thiocytisine |
title |
N-Methyl-2-thiocytisine |
title_full |
N-Methyl-2-thiocytisine |
title_fullStr |
N-Methyl-2-thiocytisine |
title_full_unstemmed |
N-Methyl-2-thiocytisine |
title_short |
N-Methyl-2-thiocytisine |
title_sort | n-methyl-2-thiocytisine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007573/ https://www.ncbi.nlm.nih.gov/pubmed/21588268 http://dx.doi.org/10.1107/S1600536810025870 |
work_keys_str_mv | AT owczarzakanitam nmethyl2thiocytisine AT przybyłannak nmethyl2thiocytisine AT kubickimaciej nmethyl2thiocytisine |