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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The shared data is the unpublished portion of the experimental section for the article with the title “NHC–Au(I) catalyzed enantioselective intramolecular [4 + 3] cycloaddition of furan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...

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Detalles Bibliográficos
Autores principales: Ma, Ruoyu, Yang, Jianbo, Kelley, Steven, Gung, Benjamin W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
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description The shared data is the unpublished portion of the experimental section for the article with the title “NHC–Au(I) catalyzed enantioselective intramolecular [4 + 3] cycloaddition of furan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.
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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complexes Ma, Ruoyu Yang, Jianbo Kelley, Steven Gung, Benjamin W. Data Brief Chemistry The shared data is the unpublished portion of the experimental section for the article with the title “NHC–Au(I) catalyzed enantioselective intramolecular [4 + 3] cycloaddition of furan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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