Dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate

In the title compound, C(14)H(16)BrNO(5), the isoxazolidine ring adopts an envelope conformation, with the N atom at the flap. In the crystal, inter­molecular C—H⋯N and C—H⋯O hydrogen bonds generate R (3) (3)(18) ring motifs which are fused into a ribbon-like structure extending along the b axis....

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Detalles Bibliográficos
Autores principales: Büyükgüngör, Orhan, Yavuz, Serkan, Odabaşoğlu, Mustafa, Özkan, Hamdi, Pamir, Özgür, Yıldırır, Yılmaz
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970144/
https://www.ncbi.nlm.nih.gov/pubmed/21577608
http://dx.doi.org/10.1107/S1600536809032462
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author Büyükgüngör, Orhan
Yavuz, Serkan
Odabaşoğlu, Mustafa
Özkan, Hamdi
Pamir, Özgür
Yıldırır, Yılmaz
author_facet Büyükgüngör, Orhan
Yavuz, Serkan
Odabaşoğlu, Mustafa
Özkan, Hamdi
Pamir, Özgür
Yıldırır, Yılmaz
author_sort Büyükgüngör, Orhan
collection PubMed
description In the title compound, C(14)H(16)BrNO(5), the isoxazolidine ring adopts an envelope conformation, with the N atom at the flap. In the crystal, inter­molecular C—H⋯N and C—H⋯O hydrogen bonds generate R (3) (3)(18) ring motifs which are fused into a ribbon-like structure extending along the b axis.
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spelling pubmed-29701442010-12-30 Dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate Büyükgüngör, Orhan Yavuz, Serkan Odabaşoğlu, Mustafa Özkan, Hamdi Pamir, Özgür Yıldırır, Yılmaz Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(16)BrNO(5), the isoxazolidine ring adopts an envelope conformation, with the N atom at the flap. In the crystal, inter­molecular C—H⋯N and C—H⋯O hydrogen bonds generate R (3) (3)(18) ring motifs which are fused into a ribbon-like structure extending along the b axis. International Union of Crystallography 2009-08-22 /pmc/articles/PMC2970144/ /pubmed/21577608 http://dx.doi.org/10.1107/S1600536809032462 Text en © Büyükgüngör et al. 2009 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
Büyükgüngör, Orhan
Yavuz, Serkan
Odabaşoğlu, Mustafa
Özkan, Hamdi
Pamir, Özgür
Yıldırır, Yılmaz
Dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate
title Dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate
title_full Dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate
title_fullStr Dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate
title_full_unstemmed Dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate
title_short Dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate
title_sort dimethyl trans-3-(4-bromo­phen­yl)-2-methyl­isoxazolidine-4,5-dicarboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970144/
https://www.ncbi.nlm.nih.gov/pubmed/21577608
http://dx.doi.org/10.1107/S1600536809032462
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