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3-(tert-Butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid
In the title compound, C(15)H(18)ClNO(4)S, the thiazolidine ring adopts a twisted conformation about the S—C(methylene) bond. The dihedral angle between the five- and six-membered rings is 77.2 (3)°. In the crystal, the molecules are linked by O—H⋯O hydrogen bonds, generating C(7) chains propagat...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983415/ https://www.ncbi.nlm.nih.gov/pubmed/21587606 http://dx.doi.org/10.1107/S1600536810037396 |
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author | Ding, Shu-Min |
author_facet | Ding, Shu-Min |
author_sort | Ding, Shu-Min |
collection | PubMed |
description | In the title compound, C(15)H(18)ClNO(4)S, the thiazolidine ring adopts a twisted conformation about the S—C(methylene) bond. The dihedral angle between the five- and six-membered rings is 77.2 (3)°. In the crystal, the molecules are linked by O—H⋯O hydrogen bonds, generating C(7) chains propagating in [100]. |
format | Text |
id | pubmed-2983415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29834152010-12-30 3-(tert-Butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid Ding, Shu-Min Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(18)ClNO(4)S, the thiazolidine ring adopts a twisted conformation about the S—C(methylene) bond. The dihedral angle between the five- and six-membered rings is 77.2 (3)°. In the crystal, the molecules are linked by O—H⋯O hydrogen bonds, generating C(7) chains propagating in [100]. International Union of Crystallography 2010-09-25 /pmc/articles/PMC2983415/ /pubmed/21587606 http://dx.doi.org/10.1107/S1600536810037396 Text en © Shu-Min Ding 2010 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 Ding, Shu-Min 3-(tert-Butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid |
title | 3-(tert-Butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid |
title_full | 3-(tert-Butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid |
title_fullStr | 3-(tert-Butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid |
title_full_unstemmed | 3-(tert-Butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid |
title_short | 3-(tert-Butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid |
title_sort | 3-(tert-butoxycarbonyl)-2-(4-chlorophenyl)-1,3-thiazolidine-4-carboxylic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983415/ https://www.ncbi.nlm.nih.gov/pubmed/21587606 http://dx.doi.org/10.1107/S1600536810037396 |
work_keys_str_mv | AT dingshumin 3tertbutoxycarbonyl24chlorophenyl13thiazolidine4carboxylicacid |