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Dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by NHC-gold(I) complexes
The shared data is the unpublished portion of the experimental section for the article with the title “NHC–Au(I) catalyzed enantioselective intramolecular [4 + 3] cycloaddition of furan propargyl esters”.[1] The preparation of the intermediates for chiral NHC-gold(I) complexes and the furan propargy...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727039/ https://www.ncbi.nlm.nih.gov/pubmed/31516945 http://dx.doi.org/10.1016/j.dib.2019.104409 |
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author | Ma, Ruoyu Yang, Jianbo Kelley, Steven Gung, Benjamin W. |
author_facet | Ma, Ruoyu Yang, Jianbo Kelley, Steven Gung, Benjamin W. |
author_sort | Ma, Ruoyu |
collection | PubMed |
description | The shared data is the unpublished portion of the experimental section for the article with the title “NHC–Au(I) catalyzed enantioselective intramolecular [4 + 3] cycloaddition of furan propargyl esters”.[1] The preparation of the intermediates for chiral NHC-gold(I) complexes and the furan propargyl ester substrates are included in this article. The (1)H NMR and (13)C NMR spectra of the gold complexes 17a-19c and the X-ray crystal data of 17a, 18a and cycloaddition product 24 are also provided in this article or in Mendeley Data. Finally, the chiral HPLC spectra used to determine enantiomeric excess and Cartesian coordinates of the optimized structure of 25 and 26 calculated by DFT calculation are also presented in the article. |
format | Online Article Text |
id | pubmed-6727039 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-67270392019-09-12 Dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by NHC-gold(I) complexes Ma, Ruoyu Yang, Jianbo Kelley, Steven Gung, Benjamin W. Data Brief Chemistry The shared data is the unpublished portion of the experimental section for the article with the title “NHC–Au(I) catalyzed enantioselective intramolecular [4 + 3] cycloaddition of furan propargyl esters”.[1] The preparation of the intermediates for chiral NHC-gold(I) complexes and the furan propargyl ester substrates are included in this article. The (1)H NMR and (13)C NMR spectra of the gold complexes 17a-19c and the X-ray crystal data of 17a, 18a and cycloaddition product 24 are also provided in this article or in Mendeley Data. Finally, the chiral HPLC spectra used to determine enantiomeric excess and Cartesian coordinates of the optimized structure of 25 and 26 calculated by DFT calculation are also presented in the article. Elsevier 2019-08-21 /pmc/articles/PMC6727039/ /pubmed/31516945 http://dx.doi.org/10.1016/j.dib.2019.104409 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Chemistry Ma, Ruoyu Yang, Jianbo Kelley, Steven Gung, Benjamin W. Dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by NHC-gold(I) complexes |
title | Dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by NHC-gold(I) complexes |
title_full | Dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by NHC-gold(I) complexes |
title_fullStr | Dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by NHC-gold(I) complexes |
title_full_unstemmed | Dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by NHC-gold(I) complexes |
title_short | Dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by NHC-gold(I) complexes |
title_sort | dataset of asymmetric intramolecular [4+3] cycloaddition reactions catalyzed by nhc-gold(i) complexes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6727039/ https://www.ncbi.nlm.nih.gov/pubmed/31516945 http://dx.doi.org/10.1016/j.dib.2019.104409 |
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