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(4R,5S)-5-Benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one
The title compound, C(13)H(18)N(2)O(2), is an N(4)-isopropyl-l-phenylalanine-based oxadiazinanone. Although the two molecules in the asymmetric unit are oriented appropriately for hydrogen bonding, the distance between the donor and acceptor atoms is large enough to support only weak, if any, hydr...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961530/ https://www.ncbi.nlm.nih.gov/pubmed/21202562 http://dx.doi.org/10.1107/S1600536808013056 |
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author | Addison, Lacey D. Dore, Delvis D. Hitchcock, Shawn R. Ferrence, Gregory M. |
author_facet | Addison, Lacey D. Dore, Delvis D. Hitchcock, Shawn R. Ferrence, Gregory M. |
author_sort | Addison, Lacey D. |
collection | PubMed |
description | The title compound, C(13)H(18)N(2)O(2), is an N(4)-isopropyl-l-phenylalanine-based oxadiazinanone. Although the two molecules in the asymmetric unit are oriented appropriately for hydrogen bonding, the distance between the donor and acceptor atoms is large enough to support only weak, if any, hydrogen bonding. The absolute configuration is known based on the known starting compounds in the synthetic procedure. |
format | Text |
id | pubmed-2961530 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29615302010-12-30 (4R,5S)-5-Benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one Addison, Lacey D. Dore, Delvis D. Hitchcock, Shawn R. Ferrence, Gregory M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(18)N(2)O(2), is an N(4)-isopropyl-l-phenylalanine-based oxadiazinanone. Although the two molecules in the asymmetric unit are oriented appropriately for hydrogen bonding, the distance between the donor and acceptor atoms is large enough to support only weak, if any, hydrogen bonding. The absolute configuration is known based on the known starting compounds in the synthetic procedure. International Union of Crystallography 2008-05-10 /pmc/articles/PMC2961530/ /pubmed/21202562 http://dx.doi.org/10.1107/S1600536808013056 Text en © Addison et al. 2008 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 Addison, Lacey D. Dore, Delvis D. Hitchcock, Shawn R. Ferrence, Gregory M. (4R,5S)-5-Benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one |
title | (4R,5S)-5-Benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one |
title_full | (4R,5S)-5-Benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one |
title_fullStr | (4R,5S)-5-Benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one |
title_full_unstemmed | (4R,5S)-5-Benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one |
title_short | (4R,5S)-5-Benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one |
title_sort | (4r,5s)-5-benzyl-4-isopropyl-1,3,4-oxadiazinan-2-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961530/ https://www.ncbi.nlm.nih.gov/pubmed/21202562 http://dx.doi.org/10.1107/S1600536808013056 |
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