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(3R,4S,5S)-4-Hydroxy-3-methyl-5-[(2S,3R)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one
The title compound, C(11)H(18)O(3), was synthesized to prove the relative configuration of the corresponding acyclic C1—C8 stereopentade. It crystallizes with two molecules in the asymmetric unit, which show only slight differences. The molecules are linked via O—H⋯O hydrogen bonds, resulting in t...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962143/ https://www.ncbi.nlm.nih.gov/pubmed/21203225 http://dx.doi.org/10.1107/S1600536808021181 |
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author | Becker, Annika Schürmann, Markus Preut, Hans Hiersemann, Martin |
author_facet | Becker, Annika Schürmann, Markus Preut, Hans Hiersemann, Martin |
author_sort | Becker, Annika |
collection | PubMed |
description | The title compound, C(11)H(18)O(3), was synthesized to prove the relative configuration of the corresponding acyclic C1—C8 stereopentade. It crystallizes with two molecules in the asymmetric unit, which show only slight differences. The molecules are linked via O—H⋯O hydrogen bonds, resulting in two crystallographically independent chains of molecules propagating in the a-axis direction. The absolute configuration was known from the synthesis. |
format | Text |
id | pubmed-2962143 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29621432010-12-30 (3R,4S,5S)-4-Hydroxy-3-methyl-5-[(2S,3R)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one Becker, Annika Schürmann, Markus Preut, Hans Hiersemann, Martin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(18)O(3), was synthesized to prove the relative configuration of the corresponding acyclic C1—C8 stereopentade. It crystallizes with two molecules in the asymmetric unit, which show only slight differences. The molecules are linked via O—H⋯O hydrogen bonds, resulting in two crystallographically independent chains of molecules propagating in the a-axis direction. The absolute configuration was known from the synthesis. International Union of Crystallography 2008-07-16 /pmc/articles/PMC2962143/ /pubmed/21203225 http://dx.doi.org/10.1107/S1600536808021181 Text en © Becker 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 Becker, Annika Schürmann, Markus Preut, Hans Hiersemann, Martin (3R,4S,5S)-4-Hydroxy-3-methyl-5-[(2S,3R)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one |
title | (3R,4S,5S)-4-Hydroxy-3-methyl-5-[(2S,3R)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one |
title_full | (3R,4S,5S)-4-Hydroxy-3-methyl-5-[(2S,3R)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one |
title_fullStr | (3R,4S,5S)-4-Hydroxy-3-methyl-5-[(2S,3R)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one |
title_full_unstemmed | (3R,4S,5S)-4-Hydroxy-3-methyl-5-[(2S,3R)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one |
title_short | (3R,4S,5S)-4-Hydroxy-3-methyl-5-[(2S,3R)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one |
title_sort | (3r,4s,5s)-4-hydroxy-3-methyl-5-[(2s,3r)-3-methylpent-4-en-2-yl]tetrahydrofuran-2-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962143/ https://www.ncbi.nlm.nih.gov/pubmed/21203225 http://dx.doi.org/10.1107/S1600536808021181 |
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