{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,2]],"date-time":"2026-09-02T13:15:34Z","timestamp":1788354934238,"version":"build-2803163510"},"reference-count":43,"publisher":"American Chemical Society (ACS)","issue":"11","license":[{"start":{"date-parts":[[2019,8,27]],"date-time":"2019-08-27T00:00:00Z","timestamp":1566864000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/pubs.acs.org\/page\/policy\/authorchoice_ccby_termsofuse.html"}],"funder":[{"DOI":"10.13039\/501100004012","name":"Jane ja Aatos Erkon S\u00e4\u00e4ti\u00f6","doi-asserted-by":"publisher","award":["NA"],"award-info":[{"award-number":["NA"]}],"id":[{"id":"10.13039\/501100004012","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2019,9,10]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>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 \u201cgreen\u201d 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.<\/jats:p>","DOI":"10.1021\/acsomega.9b02577","type":"journal-article","created":{"date-parts":[[2019,8,27]],"date-time":"2019-08-27T14:08:45Z","timestamp":1566914925000},"page":"14663-14668","source":"Crossref","is-referenced-by-count":2,"title":["(\n                    <i>E<\/i>\n                    )-Di-iodination of Alkynes\nUsing Dried Dowex H+\/NaI Approach"],"prefix":"10.1021","volume":"4","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7720-2215","authenticated-orcid":true,"given":"Juri M.","family":"Timonen","sequence":"first","affiliation":[{"name":"University of Eastern Finland , , P.O. Box 1627, ,","place":["Kuopio, Finland, FIN-70211"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7546-8906","authenticated-orcid":true,"given":"Petri A.","family":"Turhanen","sequence":"additional","affiliation":[{"name":"University of Eastern Finland , , P.O. Box 1627, ,","place":["Kuopio, Finland, FIN-70211"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"316","published-online":{"date-parts":[[2019,8,27]]},"reference":[{"key":"2026090208245792300_cit1","unstructured":"https:\/\/en.wikipedia.org\/wiki\/Green_chemistry (accessed Jul 02, 2019)."},{"key":"2026090208245792300_cit2","doi-asserted-by":"publisher","first-page":"31","DOI":"10.1039\/B711717E","article-title":"Green Chemistry Tools to Influence\na Medicinal Chemistry and Research Chemistry Based Organisation","volume":"10","author":"Alfonsi","year":"2008","journal-title":"Green Chem."},{"key":"2026090208245792300_cit3","doi-asserted-by":"publisher","first-page":"3151","DOI":"10.1080\/00397910701545171","article-title":"Facile Synthesis\nof E-Diiodoalkenes: H2O2-Activated Reaction\nof Alkynes with Iodine","volume":"37","author":"Terent\u2019ev","year":"2007","journal-title":"Synth. 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