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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...

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Detalles Bibliográficos
Autores principales: Addison, Lacey D., Dore, Delvis D., Hitchcock, Shawn R., Ferrence, Gregory M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
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.
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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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