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(E)-Di-iodination of Alkynes Using Dried Dowex H(+)/NaI Approach

[Image: see text] We investigated the usefulness of the dried Dowex H(+)/NaI approach for the selective di-iodination of alkynes. The Dowex H(+)/NaI approach selectively produces only (E)-di-iodinated products; it is very straightforward and nontoxic. The utilization of 2-propanol as a solvent in th...

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Autores principales: Timonen, Juri M., Turhanen, Petri A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741282/
https://www.ncbi.nlm.nih.gov/pubmed/31528823
http://dx.doi.org/10.1021/acsomega.9b02577
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author Timonen, Juri M.
Turhanen, Petri A.
author_facet Timonen, Juri M.
Turhanen, Petri A.
author_sort Timonen, Juri M.
collection PubMed
description [Image: see text] We investigated the usefulness of the dried Dowex H(+)/NaI approach for the selective di-iodination of alkynes. The Dowex H(+)/NaI approach selectively produces only (E)-di-iodinated products; it is very straightforward and nontoxic. The utilization of 2-propanol as a solvent in the reactions can be considered as a “green” approach and the method maybe extended to radio-iodination. The method allows access to highly important building blocks. An initial example of the di-iodination and esterification in the same one-pot reaction is also presented.
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spelling pubmed-67412822019-09-16 (E)-Di-iodination of Alkynes Using Dried Dowex H(+)/NaI Approach Timonen, Juri M. Turhanen, Petri A. ACS Omega [Image: see text] We investigated the usefulness of the dried Dowex H(+)/NaI approach for the selective di-iodination of alkynes. The Dowex H(+)/NaI approach selectively produces only (E)-di-iodinated products; it is very straightforward and nontoxic. The utilization of 2-propanol as a solvent in the reactions can be considered as a “green” approach and the method maybe extended to radio-iodination. The method allows access to highly important building blocks. An initial example of the di-iodination and esterification in the same one-pot reaction is also presented. American Chemical Society 2019-08-27 /pmc/articles/PMC6741282/ /pubmed/31528823 http://dx.doi.org/10.1021/acsomega.9b02577 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Timonen, Juri M.
Turhanen, Petri A.
(E)-Di-iodination of Alkynes Using Dried Dowex H(+)/NaI Approach
title (E)-Di-iodination of Alkynes Using Dried Dowex H(+)/NaI Approach
title_full (E)-Di-iodination of Alkynes Using Dried Dowex H(+)/NaI Approach
title_fullStr (E)-Di-iodination of Alkynes Using Dried Dowex H(+)/NaI Approach
title_full_unstemmed (E)-Di-iodination of Alkynes Using Dried Dowex H(+)/NaI Approach
title_short (E)-Di-iodination of Alkynes Using Dried Dowex H(+)/NaI Approach
title_sort (e)-di-iodination of alkynes using dried dowex h(+)/nai approach
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741282/
https://www.ncbi.nlm.nih.gov/pubmed/31528823
http://dx.doi.org/10.1021/acsomega.9b02577
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