{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T11:42:48Z","timestamp":1792496568970,"version":"4.5.0"},"reference-count":60,"publisher":"Wiley","issue":"20","license":[{"start":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T00:00:00Z","timestamp":1792454400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T00:00:00Z","timestamp":1792454400000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"funder":[{"DOI":"10.13039\/501100001871","name":"Funda\u00e7\u00e3o para a Ci\u00eancia e a Tecnologia","doi-asserted-by":"publisher","award":["2022.08851.PTDC2024.16780.PEXUID\/04138\/2025"],"award-info":[{"award-number":["2022.08851.PTDC2024.16780.PEXUID\/04138\/2025"]}],"id":[{"id":"10.13039\/501100001871","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["chemistry-europe.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["ChemSusChem"],"published-print":{"date-parts":[[2026,10,28]]},"abstract":"<jats:p>\n                    The development of sustainable synthetic methodologies is crucial to advancing greener processes. In this work, a mild and chemoselective photochemical oxidation of thiazolidines to the corresponding thiazolines under an oxygen\u2010free atmosphere and oxazolidines to oxazolines under an\u00a0oxygen atmosphere is described. The transformation proceeds efficiently with the inexpensive organophotocatalyst 9\u2010fluorenone for thiazolidines, while both [Ru(bpy)\n                    <jats:sub>3<\/jats:sub>\n                    ](PF\n                    <jats:sub>6<\/jats:sub>\n                    )\n                    <jats:sub>2<\/jats:sub>\n                    and 3CzClIPN proved effective for oxazolidines. The reaction tolerates a wide range of functional groups, including oxidation\u2010sensitive moieties such as dimethylamines and boronic acids, and delivers up to 94% yield across 28 substrates. Importantly, this methodology enables the late\u2010stage functionalization of the chitin\u2010derived synthon 3\u2010acetamido\u20105\u2010formylfuran (3A5F), a challenging aldehyde prone to decomposition, expanding the chemical space of nitrogen\u2010containing renewable scaffolds. The synthetic utility of the process is further demonstrated through the total synthesis of the antibacterial natural product Aerugine in 20% overall yield. This sustainable and versatile approach opens new avenues for the preparation of heterocycles and bioactive molecules from renewable resources.\n                  <\/jats:p>","DOI":"10.1002\/cssc.71147","type":"journal-article","created":{"date-parts":[[2026,10,20]],"date-time":"2026-10-20T11:16:32Z","timestamp":1792494992000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Photochemical Oxidation of Thiazolidines and Oxazolidines Enables Access to Reactive Oxygen Species (ROS) Sensitive and Chitin\u2010Derived Heterocycles"],"prefix":"10.1002","volume":"19","author":[{"given":"K\u00e9ssia H. S.","family":"Andrade","sequence":"first","affiliation":[{"name":"Research Institute for Medicines (iMed.ULisboa) Faculty of Pharmacy Universidade de Lisboa  Lisbon Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tiago","family":"Santos","sequence":"additional","affiliation":[{"name":"Research Institute for Medicines (iMed.ULisboa) Faculty of Pharmacy Universidade de Lisboa  Lisbon Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2677-101X","authenticated-orcid":false,"given":"Pier Giorgio","family":"Cozzi","sequence":"additional","affiliation":[{"name":"Dipartimento di Chimica \u201cGiacomo Ciamician\u201d Alma Mater Studiorum \u2013 Universit\u00e0 di Bologna  Bologna Italy"},{"name":"Center for Chemical Catalysis \u2013 C3 Alma Mater Studiorum \u2013 Universit\u00e0 di Bologna  Bologna Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2403-4216","authenticated-orcid":false,"given":"Andrea","family":"Gualandi","sequence":"additional","affiliation":[{"name":"Dipartimento di Chimica \u201cGiacomo Ciamician\u201d Alma Mater Studiorum \u2013 Universit\u00e0 di Bologna  Bologna Italy"},{"name":"Center for Chemical Catalysis \u2013 C3 Alma Mater Studiorum \u2013 Universit\u00e0 di Bologna  Bologna Italy"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-7284-5948","authenticated-orcid":false,"given":"Carlos A. M.","family":"Afonso","sequence":"additional","affiliation":[{"name":"Research Institute for Medicines (iMed.ULisboa) Faculty of Pharmacy Universidade de Lisboa  Lisbon Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2598-8540","authenticated-orcid":false,"given":"Rafael F. A.","family":"Gomes","sequence":"additional","affiliation":[{"name":"Research Institute for Medicines (iMed.ULisboa) Faculty of Pharmacy Universidade de Lisboa  Lisbon Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2026,10,20]]},"reference":[{"key":"e_1_2_8_2_1","doi-asserted-by":"crossref","first-page":"510","DOI":"10.1039\/D1GC03278J","article-title":"Furfural \u2013 a Versatile, Biomass\u2010Derived Platform Chemical for the Production of Renewable Chemicals","volume":"24","author":"Jaswal A.","year":"2022","journal-title":"Green Chemistry"},{"key":"e_1_2_8_3_1","doi-asserted-by":"crossref","first-page":"1144","DOI":"10.1039\/C5EE02666K","article-title":"Furfural: A Renewable and Versatile Platform Molecule for the Synthesis of Chemicals and Fuels","volume":"9","author":"Mariscal R.","year":"2016","journal-title":"Energy & Environmental Science"},{"key":"e_1_2_8_4_1","doi-asserted-by":"crossref","first-page":"239","DOI":"10.5267\/j.ccl.2025.1.001","article-title":"A Review on Conversions of Furfural: Gateway for Numerous Applications","volume":"14","author":"Martis G. 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