Cargando…
(6S)-2,4-Di-tert-butyl-6-[(4S,5R)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol
The title oxazolidine compound, C(27)H(39)NO(2), was synthesized from N-isopropylnorephedrine. The dihedral angle between the aromatic rings is 70.33 (5)°. The N atom of the heterocycle is oriented to allow intramolecular O—H⋯N hydrogen bonding with the hydroxy substituent.
| Autores principales: | , , , , |
|---|---|
| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2010
|
| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983885/ https://www.ncbi.nlm.nih.gov/pubmed/21580715 http://dx.doi.org/10.1107/S1600536810009074 |
| _version_ | 1782191981935460352 |
|---|---|
| author | Campbell, Ian Sean Edler, Kate L. Parrott, Raleigh W. Hitchcock, Shawn R. Ferrence, Gregory M. |
| author_facet | Campbell, Ian Sean Edler, Kate L. Parrott, Raleigh W. Hitchcock, Shawn R. Ferrence, Gregory M. |
| author_sort | Campbell, Ian Sean |
| collection | PubMed |
| description | The title oxazolidine compound, C(27)H(39)NO(2), was synthesized from N-isopropylnorephedrine. The dihedral angle between the aromatic rings is 70.33 (5)°. The N atom of the heterocycle is oriented to allow intramolecular O—H⋯N hydrogen bonding with the hydroxy substituent. |
| format | Text |
| id | pubmed-2983885 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2010 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29838852010-12-30 (6S)-2,4-Di-tert-butyl-6-[(4S,5R)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol Campbell, Ian Sean Edler, Kate L. Parrott, Raleigh W. Hitchcock, Shawn R. Ferrence, Gregory M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title oxazolidine compound, C(27)H(39)NO(2), was synthesized from N-isopropylnorephedrine. The dihedral angle between the aromatic rings is 70.33 (5)°. The N atom of the heterocycle is oriented to allow intramolecular O—H⋯N hydrogen bonding with the hydroxy substituent. International Union of Crystallography 2010-03-24 /pmc/articles/PMC2983885/ /pubmed/21580715 http://dx.doi.org/10.1107/S1600536810009074 Text en © Campbell 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 Campbell, Ian Sean Edler, Kate L. Parrott, Raleigh W. Hitchcock, Shawn R. Ferrence, Gregory M. (6S)-2,4-Di-tert-butyl-6-[(4S,5R)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol |
| title | (6S)-2,4-Di-tert-butyl-6-[(4S,5R)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol |
| title_full | (6S)-2,4-Di-tert-butyl-6-[(4S,5R)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol |
| title_fullStr | (6S)-2,4-Di-tert-butyl-6-[(4S,5R)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol |
| title_full_unstemmed | (6S)-2,4-Di-tert-butyl-6-[(4S,5R)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol |
| title_short | (6S)-2,4-Di-tert-butyl-6-[(4S,5R)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol |
| title_sort | (6s)-2,4-di-tert-butyl-6-[(4s,5r)-3-isopropyl-4-methyl-5-phenyloxazolidin-2-yl]phenol |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983885/ https://www.ncbi.nlm.nih.gov/pubmed/21580715 http://dx.doi.org/10.1107/S1600536810009074 |
| work_keys_str_mv | AT campbelliansean 6s24ditertbutyl64s5r3isopropyl4methyl5phenyloxazolidin2ylphenol AT edlerkatel 6s24ditertbutyl64s5r3isopropyl4methyl5phenyloxazolidin2ylphenol AT parrottraleighw 6s24ditertbutyl64s5r3isopropyl4methyl5phenyloxazolidin2ylphenol AT hitchcockshawnr 6s24ditertbutyl64s5r3isopropyl4methyl5phenyloxazolidin2ylphenol AT ferrencegregorym 6s24ditertbutyl64s5r3isopropyl4methyl5phenyloxazolidin2ylphenol |