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(6S)-2-tert-Butyl-6-[(4S,5R)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol
The title compound, C(21)H(27)NO(2), exhibits hydrogen bonding between the phenolic H atom and the heterocyclic N atom. The absolute configuration of the molecule is known from the synthetic procedure.
| Autores principales: | , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2010
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983802/ https://www.ncbi.nlm.nih.gov/pubmed/21580716 http://dx.doi.org/10.1107/S1600536810009190 |
| _version_ | 1782191961665437696 |
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| author | Anderson, Alexander E. Edler, Kate L. Parrott, Raleigh W. Hitchcock, Shawn R. Ferrence, Gregory M. |
| author_facet | Anderson, Alexander E. Edler, Kate L. Parrott, Raleigh W. Hitchcock, Shawn R. Ferrence, Gregory M. |
| author_sort | Anderson, Alexander E. |
| collection | PubMed |
| description | The title compound, C(21)H(27)NO(2), exhibits hydrogen bonding between the phenolic H atom and the heterocyclic N atom. The absolute configuration of the molecule is known from the synthetic procedure. |
| format | Text |
| id | pubmed-2983802 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2010 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29838022010-12-30 (6S)-2-tert-Butyl-6-[(4S,5R)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol Anderson, Alexander E. Edler, Kate L. Parrott, Raleigh W. Hitchcock, Shawn R. Ferrence, Gregory M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(21)H(27)NO(2), exhibits hydrogen bonding between the phenolic H atom and the heterocyclic N atom. The absolute configuration of the molecule is known from the synthetic procedure. International Union of Crystallography 2010-03-24 /pmc/articles/PMC2983802/ /pubmed/21580716 http://dx.doi.org/10.1107/S1600536810009190 Text en © Anderson 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 Anderson, Alexander E. Edler, Kate L. Parrott, Raleigh W. Hitchcock, Shawn R. Ferrence, Gregory M. (6S)-2-tert-Butyl-6-[(4S,5R)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol |
| title | (6S)-2-tert-Butyl-6-[(4S,5R)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol |
| title_full | (6S)-2-tert-Butyl-6-[(4S,5R)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol |
| title_fullStr | (6S)-2-tert-Butyl-6-[(4S,5R)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol |
| title_full_unstemmed | (6S)-2-tert-Butyl-6-[(4S,5R)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol |
| title_short | (6S)-2-tert-Butyl-6-[(4S,5R)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol |
| title_sort | (6s)-2-tert-butyl-6-[(4s,5r)-3,4-dimethyl-5-phenyloxazolidin-2-yl]phenol |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983802/ https://www.ncbi.nlm.nih.gov/pubmed/21580716 http://dx.doi.org/10.1107/S1600536810009190 |
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