tert-Butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate

The title compound, C(10)H(15)NO(4), also known as N-tert-butyl­oxycarbonyl-allohydr­oxy-l-proline lactone, is quite similar to N-acetyl-allohydr­oxy-l-proline lactone [Lenstra, Petit & Geise (1979 ▶). Cryst. Struct. Commun. 8, 1023–1029], whereby both carbonyl groups point roughly in the same d...

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Detalles Bibliográficos
Autores principales: Lechner, Marie-Charlotte, Aubert, Emmanuel, Guichard, Gilles, Didierjean, Claude
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959344/
https://www.ncbi.nlm.nih.gov/pubmed/21201231
http://dx.doi.org/10.1107/S1600536808030651
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author Lechner, Marie-Charlotte
Aubert, Emmanuel
Guichard, Gilles
Didierjean, Claude
author_facet Lechner, Marie-Charlotte
Aubert, Emmanuel
Guichard, Gilles
Didierjean, Claude
author_sort Lechner, Marie-Charlotte
collection PubMed
description The title compound, C(10)H(15)NO(4), also known as N-tert-butyl­oxycarbonyl-allohydr­oxy-l-proline lactone, is quite similar to N-acetyl-allohydr­oxy-l-proline lactone [Lenstra, Petit & Geise (1979 ▶). Cryst. Struct. Commun. 8, 1023–1029], whereby both carbonyl groups point roughly in the same direction because of the trans conformation of the peptide bond.
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spelling pubmed-29593442010-12-30 tert-Butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate Lechner, Marie-Charlotte Aubert, Emmanuel Guichard, Gilles Didierjean, Claude Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(10)H(15)NO(4), also known as N-tert-butyl­oxycarbonyl-allohydr­oxy-l-proline lactone, is quite similar to N-acetyl-allohydr­oxy-l-proline lactone [Lenstra, Petit & Geise (1979 ▶). Cryst. Struct. Commun. 8, 1023–1029], whereby both carbonyl groups point roughly in the same direction because of the trans conformation of the peptide bond. International Union of Crystallography 2008-09-30 /pmc/articles/PMC2959344/ /pubmed/21201231 http://dx.doi.org/10.1107/S1600536808030651 Text en © Lechner 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
Lechner, Marie-Charlotte
Aubert, Emmanuel
Guichard, Gilles
Didierjean, Claude
tert-Butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate
title tert-Butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate
title_full tert-Butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate
title_fullStr tert-Butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate
title_full_unstemmed tert-Butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate
title_short tert-Butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate
title_sort tert-butyl 3-oxo-2-oxa-5-aza­bicyclo­[2.2.1]heptane-5-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959344/
https://www.ncbi.nlm.nih.gov/pubmed/21201231
http://dx.doi.org/10.1107/S1600536808030651
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