{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T22:14:30Z","timestamp":1787004870112,"version":"build-2736575974"},"reference-count":55,"publisher":"Georg Thieme Verlag KG","issue":"13","license":[{"start":{"date-parts":[[2025,5,5]],"date-time":"2025-05-05T00:00:00Z","timestamp":1746403200000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"funder":[{"DOI":"10.13039\/100000057","name":"National Institute of General Medical Sciences","doi-asserted-by":"crossref","award":["1R35GM154965"],"award-info":[{"award-number":["1R35GM154965"]}],"id":[{"id":"10.13039\/100000057","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"crossref"}]},{"DOI":"10.13039\/100010842","name":"Temple University","doi-asserted-by":"crossref","id":[{"id":"10.13039\/100010842","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Synlett"],"published-print":{"date-parts":[[2025,8]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Protecting groups are commonplace in organic synthesis and appear often in the form of dioxanes and dioxolanes. 1,3-Dioxolanes can be used for the protection of both diol and carbonyl motifs. Our group has been increasingly interested in alternative uses for such a simple and often overlooked heterocycle. Herein we highlight recent advancements in dioxolanyl radical chemistry where reactivity can be selectively directed towards two unique positions leading to distinct product formations, resulting in trifluoromethyl ketones and 1,2-diol functionalities.<\/jats:p>\n                  <jats:p>1 \tIntroduction<\/jats:p>\n                  <jats:p>2 \tDioxolanyl Radicals: Masked Trifluoromethylacetylation<\/jats:p>\n                  <jats:p>3 \tDioxolanyl Radicals: Vicinal Functionality<\/jats:p>\n                  <jats:p>4 \tConclusion and Outlook<\/jats:p>","DOI":"10.1055\/a-2599-8435","type":"journal-article","created":{"date-parts":[[2025,5,5]],"date-time":"2025-05-05T18:57:12Z","timestamp":1746471432000},"page":"1799-1807","source":"Crossref","is-referenced-by-count":2,"title":["The Duality of Dioxolanyl Radicals towards C\u2013C Bond Construction"],"prefix":"10.1055","volume":"36","author":[{"given":"Kyra L.","family":"Samony","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Justin J.","family":"Chang","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0667-6170","authenticated-orcid":false,"given":"Daniel K.","family":"Kim","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"194","published-online":{"date-parts":[[2025,5,19]]},"reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"7271","DOI":"10.1021\/acsomega.4c00948","volume":"9","author":"P Mainkar","year":"2024","journal-title":"ACS Omega"},{"key":"ref2","doi-asserted-by":"crossref","first-page":"2790","DOI":"10.1039\/D3GC00227F","volume":"25","author":"M Melchiorre","year":"2023","journal-title":"Green Chem."},{"key":"ref3","doi-asserted-by":"crossref","first-page":"3180","DOI":"10.1021\/acsenergylett.3c01004","volume":"8","author":"Y Zhao","year":"2023","journal-title":"ACS Energy Lett."},{"key":"ref4","doi-asserted-by":"crossref","first-page":"4974","DOI":"10.1021\/acsomega.8b00159","volume":"3","author":"J L Dong","year":"2018","journal-title":"ACS Omega"},{"key":"ref5","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1007\/s11743-998-0010-x","volume":"1","author":"K Urata","year":"1998","journal-title":"J. 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