2,6-Bis[(S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine

The commercially available title compound, C(25)H(23)N(3)O(2), has been known since 1993 [Nesper et al. (1993 ▶). Helv. Chim. Acta, 76, 2239–2249], but has not been structurally characterized until now. In the free ligand, the N atoms of both oxazoline rings point in opposite directions. The phenyl...

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Detalles Bibliográficos
Autores principales: Möller, Konstanze, Junge, Kathrin, Spannenberg, Anke, Beller, Matthias
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089107/
https://www.ncbi.nlm.nih.gov/pubmed/21754484
http://dx.doi.org/10.1107/S1600536811014061
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author Möller, Konstanze
Junge, Kathrin
Spannenberg, Anke
Beller, Matthias
author_facet Möller, Konstanze
Junge, Kathrin
Spannenberg, Anke
Beller, Matthias
author_sort Möller, Konstanze
collection PubMed
description The commercially available title compound, C(25)H(23)N(3)O(2), has been known since 1993 [Nesper et al. (1993 ▶). Helv. Chim. Acta, 76, 2239–2249], but has not been structurally characterized until now. In the free ligand, the N atoms of both oxazoline rings point in opposite directions. The phenyl rings make dihedral angles of 30.56 (5) and 84.57 (3)° with the pyridine ring and 72.85 (3)° with each other.
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spelling pubmed-30891072011-07-13 2,6-Bis[(S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine Möller, Konstanze Junge, Kathrin Spannenberg, Anke Beller, Matthias Acta Crystallogr Sect E Struct Rep Online Organic Papers The commercially available title compound, C(25)H(23)N(3)O(2), has been known since 1993 [Nesper et al. (1993 ▶). Helv. Chim. Acta, 76, 2239–2249], but has not been structurally characterized until now. In the free ligand, the N atoms of both oxazoline rings point in opposite directions. The phenyl rings make dihedral angles of 30.56 (5) and 84.57 (3)° with the pyridine ring and 72.85 (3)° with each other. International Union of Crystallography 2011-04-22 /pmc/articles/PMC3089107/ /pubmed/21754484 http://dx.doi.org/10.1107/S1600536811014061 Text en © Möller 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
Möller, Konstanze
Junge, Kathrin
Spannenberg, Anke
Beller, Matthias
2,6-Bis[(S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine
title 2,6-Bis[(S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine
title_full 2,6-Bis[(S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine
title_fullStr 2,6-Bis[(S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine
title_full_unstemmed 2,6-Bis[(S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine
title_short 2,6-Bis[(S)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine
title_sort 2,6-bis[(s)-4-benzyl-4,5-dihydro-1,3-oxazol-2-yl]pyridine
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089107/
https://www.ncbi.nlm.nih.gov/pubmed/21754484
http://dx.doi.org/10.1107/S1600536811014061
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AT jungekathrin 26biss4benzyl45dihydro13oxazol2ylpyridine
AT spannenberganke 26biss4benzyl45dihydro13oxazol2ylpyridine
AT bellermatthias 26biss4benzyl45dihydro13oxazol2ylpyridine

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