(2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate

The title compound, C(13)H(12)BrNO(4), was obtained from an optically active aniline derivative. The structure was characterized by (1)H NMR, (13)C NMR, MS and X-ray diffraction techniques. 86% of the atoms of the two independent mol­ecules in the asymmetric unit show non-crystallographic inversion...

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Detalles Bibliográficos
Autores principales: Kurkin, Alexander V., Bernovskaya, Anna A., Yurovskaya, Marina A., Rybakov, Victor B.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961954/
https://www.ncbi.nlm.nih.gov/pubmed/21203163
http://dx.doi.org/10.1107/S1600536808020588
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author Kurkin, Alexander V.
Bernovskaya, Anna A.
Yurovskaya, Marina A.
Rybakov, Victor B.
author_facet Kurkin, Alexander V.
Bernovskaya, Anna A.
Yurovskaya, Marina A.
Rybakov, Victor B.
author_sort Kurkin, Alexander V.
collection PubMed
description The title compound, C(13)H(12)BrNO(4), was obtained from an optically active aniline derivative. The structure was characterized by (1)H NMR, (13)C NMR, MS and X-ray diffraction techniques. 86% of the atoms of the two independent mol­ecules in the asymmetric unit show non-crystallographic inversion symmetry.
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spelling pubmed-29619542010-12-30 (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate Kurkin, Alexander V. Bernovskaya, Anna A. Yurovskaya, Marina A. Rybakov, Victor B. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(12)BrNO(4), was obtained from an optically active aniline derivative. The structure was characterized by (1)H NMR, (13)C NMR, MS and X-ray diffraction techniques. 86% of the atoms of the two independent mol­ecules in the asymmetric unit show non-crystallographic inversion symmetry. International Union of Crystallography 2008-07-09 /pmc/articles/PMC2961954/ /pubmed/21203163 http://dx.doi.org/10.1107/S1600536808020588 Text en © Kurkin 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
Kurkin, Alexander V.
Bernovskaya, Anna A.
Yurovskaya, Marina A.
Rybakov, Victor B.
(2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate
title (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate
title_full (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate
title_fullStr (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate
title_full_unstemmed (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate
title_short (2R)-Ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate
title_sort (2r)-ethyl 2-(5-bromo-2,3-dioxoindolin-1-yl)propanoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961954/
https://www.ncbi.nlm.nih.gov/pubmed/21203163
http://dx.doi.org/10.1107/S1600536808020588
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