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Adamantane-1-thioamide
The title compound, C(11)H(17)NS, is an important intermediate for the synthesis of biologically active adamantlythiazolo-oxadiazoles. The adamantyl residue is disordered about a twofold rotation axis over two sites with site-occupation factors of 0.817 (3) and 0.183 (3). The crystal structure is...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977118/ https://www.ncbi.nlm.nih.gov/pubmed/21583581 http://dx.doi.org/10.1107/S1600536809027470 |
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author | Zahid, Maryam Khawar Rauf, M. Bolte, Michael Hameed, Shahid |
author_facet | Zahid, Maryam Khawar Rauf, M. Bolte, Michael Hameed, Shahid |
author_sort | Zahid, Maryam |
collection | PubMed |
description | The title compound, C(11)H(17)NS, is an important intermediate for the synthesis of biologically active adamantlythiazolo-oxadiazoles. The adamantyl residue is disordered about a twofold rotation axis over two sites with site-occupation factors of 0.817 (3) and 0.183 (3). The crystal structure is stabilized by intermolecular N—H⋯S hydrogen-bonding interactions. |
format | Text |
id | pubmed-2977118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29771182010-12-30 Adamantane-1-thioamide Zahid, Maryam Khawar Rauf, M. Bolte, Michael Hameed, Shahid Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(17)NS, is an important intermediate for the synthesis of biologically active adamantlythiazolo-oxadiazoles. The adamantyl residue is disordered about a twofold rotation axis over two sites with site-occupation factors of 0.817 (3) and 0.183 (3). The crystal structure is stabilized by intermolecular N—H⋯S hydrogen-bonding interactions. International Union of Crystallography 2009-07-18 /pmc/articles/PMC2977118/ /pubmed/21583581 http://dx.doi.org/10.1107/S1600536809027470 Text en © Zahid et al. 2009 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 Zahid, Maryam Khawar Rauf, M. Bolte, Michael Hameed, Shahid Adamantane-1-thioamide |
title | Adamantane-1-thioamide |
title_full | Adamantane-1-thioamide |
title_fullStr | Adamantane-1-thioamide |
title_full_unstemmed | Adamantane-1-thioamide |
title_short | Adamantane-1-thioamide |
title_sort | adamantane-1-thioamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977118/ https://www.ncbi.nlm.nih.gov/pubmed/21583581 http://dx.doi.org/10.1107/S1600536809027470 |
work_keys_str_mv | AT zahidmaryam adamantane1thioamide AT khawarraufm adamantane1thioamide AT boltemichael adamantane1thioamide AT hameedshahid adamantane1thioamide |