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l-2-Nitrimino-1,3-diazepane-4-carboxylic acid

The cyclic form of l-nitro­arginine, C(6)H(10)N(4)O(4), crystallizes with two independent mol­ecules in the asymmetric unit. According to the geometrical parameters, similar in both mol­ecules, the structure corresponds to that of l-2-nitrimino-1,3-diazepane-4-carboxylic acid; there are, however, co...

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Autor principal: Karapetyan, Harutyun A.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961324/
https://www.ncbi.nlm.nih.gov/pubmed/21202424
http://dx.doi.org/10.1107/S1600536808011835
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author Karapetyan, Harutyun A.
author_facet Karapetyan, Harutyun A.
author_sort Karapetyan, Harutyun A.
collection PubMed
description The cyclic form of l-nitro­arginine, C(6)H(10)N(4)O(4), crystallizes with two independent mol­ecules in the asymmetric unit. According to the geometrical parameters, similar in both mol­ecules, the structure corresponds to that of l-2-nitrimino-1,3-diazepane-4-carboxylic acid; there are, however, conformational differences between the independent molecules, one of them being close to a twisted chair while the other might be described as a rather flattened boat. All six active H atoms in the two molecules are involved in hydrogen bonds, two of which are intra­molecular and four inter­molecular, forming an infinite chain of mol­ecules along the b axis.
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spelling pubmed-29613242010-12-30 l-2-Nitrimino-1,3-diazepane-4-carboxylic acid Karapetyan, Harutyun A. Acta Crystallogr Sect E Struct Rep Online Organic Papers The cyclic form of l-nitro­arginine, C(6)H(10)N(4)O(4), crystallizes with two independent mol­ecules in the asymmetric unit. According to the geometrical parameters, similar in both mol­ecules, the structure corresponds to that of l-2-nitrimino-1,3-diazepane-4-carboxylic acid; there are, however, conformational differences between the independent molecules, one of them being close to a twisted chair while the other might be described as a rather flattened boat. All six active H atoms in the two molecules are involved in hydrogen bonds, two of which are intra­molecular and four inter­molecular, forming an infinite chain of mol­ecules along the b axis. International Union of Crystallography 2008-04-30 /pmc/articles/PMC2961324/ /pubmed/21202424 http://dx.doi.org/10.1107/S1600536808011835 Text en © Harutyun A. Karapetyan 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
Karapetyan, Harutyun A.
l-2-Nitrimino-1,3-diazepane-4-carboxylic acid
title l-2-Nitrimino-1,3-diazepane-4-carboxylic acid
title_full l-2-Nitrimino-1,3-diazepane-4-carboxylic acid
title_fullStr l-2-Nitrimino-1,3-diazepane-4-carboxylic acid
title_full_unstemmed l-2-Nitrimino-1,3-diazepane-4-carboxylic acid
title_short l-2-Nitrimino-1,3-diazepane-4-carboxylic acid
title_sort l-2-nitrimino-1,3-diazepane-4-carboxylic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961324/
https://www.ncbi.nlm.nih.gov/pubmed/21202424
http://dx.doi.org/10.1107/S1600536808011835
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