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(4R)-4-(2-Allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose
X-ray crystallography unequivocally confirmed the structure of the title compound, C(12)H(17)N(3)O(4), as (4R)-4-(2-allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose. The absolute configuration was determined by the use of d-glucorono-3,6-lactone as the starting material. The crystal stru...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959937/ https://www.ncbi.nlm.nih.gov/pubmed/21581334 http://dx.doi.org/10.1107/S1600536808036416 |
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author | Jenkinson, Sarah F. Best, Daniel Wilson, Francis X. Fleet, George W. J. Watkin, David J. |
author_facet | Jenkinson, Sarah F. Best, Daniel Wilson, Francis X. Fleet, George W. J. Watkin, David J. |
author_sort | Jenkinson, Sarah F. |
collection | PubMed |
description | X-ray crystallography unequivocally confirmed the structure of the title compound, C(12)H(17)N(3)O(4), as (4R)-4-(2-allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose. The absolute configuration was determined by the use of d-glucorono-3,6-lactone as the starting material. The crystal structure consists of hydrogen-bonded chains of molecules running parallel to the a axis. There are no unusual packing features. |
format | Text |
id | pubmed-2959937 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29599372010-12-30 (4R)-4-(2-Allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose Jenkinson, Sarah F. Best, Daniel Wilson, Francis X. Fleet, George W. J. Watkin, David J. Acta Crystallogr Sect E Struct Rep Online Organic Papers X-ray crystallography unequivocally confirmed the structure of the title compound, C(12)H(17)N(3)O(4), as (4R)-4-(2-allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose. The absolute configuration was determined by the use of d-glucorono-3,6-lactone as the starting material. The crystal structure consists of hydrogen-bonded chains of molecules running parallel to the a axis. There are no unusual packing features. International Union of Crystallography 2008-11-13 /pmc/articles/PMC2959937/ /pubmed/21581334 http://dx.doi.org/10.1107/S1600536808036416 Text en © Jenkinson 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 Jenkinson, Sarah F. Best, Daniel Wilson, Francis X. Fleet, George W. J. Watkin, David J. (4R)-4-(2-Allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose |
title | (4R)-4-(2-Allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose |
title_full | (4R)-4-(2-Allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose |
title_fullStr | (4R)-4-(2-Allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose |
title_full_unstemmed | (4R)-4-(2-Allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose |
title_short | (4R)-4-(2-Allyl-2H-1,2,3-triazol-4-yl)-1,2-O-isopropylidene-l-threose |
title_sort | (4r)-4-(2-allyl-2h-1,2,3-triazol-4-yl)-1,2-o-isopropylidene-l-threose |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959937/ https://www.ncbi.nlm.nih.gov/pubmed/21581334 http://dx.doi.org/10.1107/S1600536808036416 |
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