{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T10:30:30Z","timestamp":1793356230117,"version":"4.5.0"},"reference-count":55,"publisher":"American Chemical Society (ACS)","issue":"43","license":[{"start":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T00:00:00Z","timestamp":1791158400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T00:00:00Z","timestamp":1791158400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2026,10,5]],"date-time":"2026-10-05T00:00:00Z","timestamp":1791158400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-045"}],"funder":[{"DOI":"10.13039\/501100001809","name":"National Natural Science Foundation of China","doi-asserted-by":"publisher","award":["22361021"],"award-info":[{"award-number":["22361021"]}],"id":[{"id":"10.13039\/501100001809","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,10,30]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Herein, we report a visible-light-mediated photoredox reaction for the synthesis of sulfonyl 4-(thio)chromones and 4-quinolone derivatives. This transformation employs easily accessible 2-alkynyl benzaldehydes and sodium sulfinates as starting materials, enabling a one-pot cascade process involving radical sulfonylation, cyclization, and isomerization under mild conditions. Notably, this strategy allows the straightforward assembly of protecting-group-free sulfonyl 4-quinolones. Benefiting from its operational simplicity, broad substrate scope, and excellent functional group compatibility, this protocol provides a practical approach for the construction of valuable 4-(thio)chromones and 4-quinolone derivatives with potential biological and synthetic applications<\/jats:p>","DOI":"10.1021\/acs.joc.6c01871","type":"journal-article","created":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T00:01:27Z","timestamp":1791244887000},"page":"14454-14464","source":"Crossref","is-referenced-by-count":0,"title":["Visible-Light-Induced Synthesis for Sulfonyl (Thio)chromones and 4-Quinolones from 2-Alknyl Benzaldehydes and Sodium Sulfinates\n                    <i>via<\/i>\n                    a Cascade Sulfonylation\/Cyclization\/Isomerization Processes"],"prefix":"10.1021","volume":"91","author":[{"given":"Zhengyu","family":"Jiang","sequence":"first","affiliation":[{"name":"Jiangxi Normal University , , , ,","place":["Nanchang, Jiangxi, China, 330022"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Zhaohui","family":"Xu","sequence":"additional","affiliation":[{"name":"Jiangxi Normal University , , , ,","place":["Nanchang, Jiangxi, China, 330022"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1991-792X","authenticated-orcid":true,"given":"Qing-Yan","family":"Liu","sequence":"additional","affiliation":[{"name":"Jiangxi Normal University , , , ,","place":["Nanchang, Jiangxi, China, 330022"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0235-1432","authenticated-orcid":true,"given":"Junmin","family":"Chen","sequence":"additional","affiliation":[{"name":"Jiangxi Normal University , , , ,","place":["Nanchang, Jiangxi, China, 330022"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"316","published-online":{"date-parts":[[2026,10,5]]},"reference":[{"key":"2026103005080997200_cit1a","doi-asserted-by":"publisher","first-page":"1746","DOI":"10.2174\/092986709788186156","article-title":"The 4-Quinolone-3-Carboxylic Acid Motif as a Multivalent Scaffold in Medicinal Chemistry","volume":"16","author":"Mugnaini","year":"2009","journal-title":"Curr. Med. Chem."},{"key":"2026103005080997200_cit1b","doi-asserted-by":"publisher","DOI":"10.1016\/j.bmcl.2019.07.048","article-title":"Recent Advances in Natural Antifungal Flavonoids and Their Derivatives","volume":"29","author":"Jin","year":"2019","journal-title":"Bioorg. Med. Chem. Lett."},{"key":"2026103005080997200_cit1c","doi-asserted-by":"publisher","first-page":"3717","DOI":"10.1021\/cr100446h","article-title":"Xanthones from Fungi, Lichens, and Bacteria: The Natural Products and Their Synthesis","volume":"112","author":"Masters","year":"2012","journal-title":"Chem. Rev."},{"key":"2026103005080997200_cit1d","doi-asserted-by":"publisher","first-page":"3825","DOI":"10.2174\/092986711803414359","article-title":"An Update on Natural Occurrence and Biological Activity of Chromones","volume":"18","author":"Sharma","year":"2011","journal-title":"Curr. Med. Chem."},{"key":"2026103005080997200_cit1e","doi-asserted-by":"publisher","first-page":"12","DOI":"10.1016\/j.ajps.2017.08.004","article-title":"Bioactive Flavonoids in Medicinal Plants: Structure, Activity and Biological Fate","volume":"13","author":"Wang","year":"2018","journal-title":"Asian J. Pharm. Sci."},{"key":"2026103005080997200_cit1f","doi-asserted-by":"publisher","first-page":"4960","DOI":"10.1021\/cr400265z","article-title":"Chromone: A Valid Scaffold in Medicinal Chemistry","volume":"114","author":"Gaspar","year":"2014","journal-title":"Chem. Rev."},{"key":"2026103005080997200_cit1g","doi-asserted-by":"publisher","first-page":"7941","DOI":"10.1021\/acs.jmedchem.6b01720","article-title":"Chromone as a Privileged Scaffold in Drug Discovery: Recent Advances","volume":"60","author":"Reis","year":"2017","journal-title":"J. Med. Chem."},{"key":"2026103005080997200_cit2","doi-asserted-by":"publisher","first-page":"225","DOI":"10.1007\/s002230001123","article-title":"Ipriflavone, a Synthetic Phytoestrogen, Enhances Intestinal Calcium Transport In Vitro","volume":"67","author":"Arjmandi","year":"2000","journal-title":"Calcif. Tissue Int."},{"key":"2026103005080997200_cit3","doi-asserted-by":"publisher","first-page":"340","DOI":"10.1016\/j.ejmech.2014.03.047","article-title":"Chromones as a Privileged Scaffold in Drug Discovery: A Review","volume":"78","author":"Keri","year":"2014","journal-title":"Eur. J. Med. Chem."},{"key":"2026103005080997200_cit4","doi-asserted-by":"publisher","first-page":"1731","DOI":"10.1021\/np020204o","article-title":"Five New Homoisoflavonoids from the Tuber of Ophiopogon japonicus","volume":"65","author":"Chang","year":"2002","journal-title":"J. Nat. Prod."},{"key":"2026103005080997200_cit5a","doi-asserted-by":"publisher","first-page":"152","DOI":"10.1021\/cr100063u","article-title":"4-Quinolones: Smart Phones of the Microbial World","volume":"111","author":"Huse","year":"2011","journal-title":"Chem. Rev."},{"key":"2026103005080997200_cit5b","doi-asserted-by":"publisher","first-page":"1657","DOI":"10.1016\/s0968-0896(98)00141-2","article-title":"Synthesis and Antiplatelet Activity of Phenyl Quinolones","volume":"6","author":"Huang","year":"1998","journal-title":"Bioorg. Med. Chem."},{"key":"2026103005080997200_cit5c","doi-asserted-by":"publisher","first-page":"4205","DOI":"10.1021\/jm201642z","article-title":"Lead Optimization of 3-Carboxyl-4(1H)-quinolones to Deliver Orally Bioavailable Antimalarials","volume":"55","author":"Zhang","year":"2012","journal-title":"J. Med. Chem."},{"key":"2026103005080997200_cit5d","doi-asserted-by":"publisher","first-page":"1295","DOI":"10.1517\/13543776.2010.505922","article-title":"New Quinolone Antibiotics: A Survey of the Literature from 2005 to 2010","volume":"20","author":"Wiles","year":"2010","journal-title":"Expert Opin. Ther. Pat."},{"key":"2026103005080997200_cit5e","doi-asserted-by":"publisher","DOI":"10.1016\/j.ejmech.2026.118783","article-title":"2- and 4-Quinolones as Emerging Anticancer Scaffolds: Recent Synthetic Developments, SAR Insights, and Mechanistic Perspective","volume":"310","author":"Thadkapally","year":"2026","journal-title":"Eur. J. Med. Chem."},{"key":"2026103005080997200_cit6","doi-asserted-by":"publisher","first-page":"639","DOI":"10.1128\/AAC.29.4.639","article-title":"Genetic and Biochemical Characterization of Norfloxacin Resistance in Escherichia coli","volume":"29","author":"Hooper","year":"1986","journal-title":"Antimicrob. Agents Chemother."},{"key":"2026103005080997200_cit7","doi-asserted-by":"publisher","first-page":"441","DOI":"10.3797\/scipharm.1401-14","article-title":"Formulation and In Vitro Evaluation of Ofloxacin Tablets Using Natural Gums as Binders","volume":"82","author":"Mistry","year":"2014","journal-title":"Sci. Pharm."},{"key":"2026103005080997200_cit8","doi-asserted-by":"publisher","first-page":"9776","DOI":"10.1021\/jm5012808","article-title":"Discovery of N-(2,4-Di-tert-butyl-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide (VX-770, Ivacaftor), a Potent and Orally Bioavailable CFTR Potentiator","volume":"57","author":"Hadida","year":"2014","journal-title":"J. Med. Chem."},{"key":"2026103005080997200_cit9","doi-asserted-by":"publisher","first-page":"4883","DOI":"10.1021\/jm900456w","article-title":"Design and Synthesis of 2-(3-Benzo[b]thienyl)-6,7-methylenedioxyquinolin-4-one Analogues as Potent Antitumor Agents that Inhibit Tubulin Assembly","volume":"52","author":"Chang","year":"2009","journal-title":"J. Med. Chem."},{"key":"2026103005080997200_cit10","doi-asserted-by":"publisher","first-page":"3818","DOI":"10.1021\/jm500147k","article-title":"Discovery, Synthesis, and Optimization of Antimalarial 4(1H)-Quinolone-3-Diarylethers","volume":"57","author":"Nilsen","year":"2014","journal-title":"J. Med. Chem."},{"key":"2026103005080997200_cit11","doi-asserted-by":"publisher","first-page":"4991","DOI":"10.1016\/S0040-4039(01)80563-3","article-title":"Pumiloside and Deoxypumiloside; Plausible Intermediates of Camptothecin Biosynthesis","volume":"30","author":"Aimi","year":"1989","journal-title":"Tetrahedron Lett."},{"key":"2026103005080997200_cit12","doi-asserted-by":"publisher","first-page":"4874","DOI":"10.1021\/jm501881c","article-title":"Origins of the Quinolone Class of Antibacterials: An Expanded \u201cDiscovery Story\u201d Miniperspective","volume":"58","author":"Bisacchi","year":"2015","journal-title":"J. Med. Chem."},{"key":"2026103005080997200_cit13a","doi-asserted-by":"publisher","first-page":"3935","DOI":"10.1039\/D0QO01175D","article-title":"Metal-Free Synthesis of 3-Chalcogenyl Chromones from Alkynyl Aryl Ketones and Diorganyl Diselenides\/Disulfides Mediated by PIFA","volume":"7","author":"Ai","year":"2020","journal-title":"Org. Chem. Front."},{"key":"2026103005080997200_cit13b","doi-asserted-by":"publisher","first-page":"5104","DOI":"10.1039\/d2ob00696k","article-title":"Silver-Catalysed Three-Component Reactions of Alkynyl Aryl Ketones, Element Selenium, and Boronic Acids Leading to 3-Organoselenylchromones","volume":"20","author":"Lai","year":"2022","journal-title":"Org. Biomol. Chem."},{"key":"2026103005080997200_cit13c","doi-asserted-by":"publisher","first-page":"16441","DOI":"10.1039\/C9NJ04580E","article-title":"PIDA-Mediated \u03b1-C\u2013H Functionalization of Enaminones: The Synthesis of Thiocyano Enaminones and Chromones in Water","volume":"43","author":"Yang","year":"2019","journal-title":"New J. Chem."},{"key":"2026103005080997200_cit13d","doi-asserted-by":"publisher","first-page":"5397","DOI":"10.1002\/cctc.201801548","article-title":"NIS\/TBHP Induced Regioselective Selenation of (Hetero)Arenes via Direct C\u2013H Functionalization","volume":"10","author":"Ding","year":"2018","journal-title":"ChemCatChem"},{"key":"2026103005080997200_cit13e","doi-asserted-by":"publisher","first-page":"198","DOI":"10.1016\/j.gresc.2021.12.003","article-title":"Synthesis of 3-Thiocyanated Chromones via TCCA\/NH4SCN Mediated Cyclization\/Thiocyanation of Alkynyl Aryl Ketones","volume":"3","author":"Xiao","year":"2022","journal-title":"Green Synth. Catal."},{"key":"2026103005080997200_cit13f","doi-asserted-by":"publisher","DOI":"10.1016\/j.cclet.2024.110784","article-title":"An Update on the Advances in Chromone and the Derivatives Synthesis Based on the Key Chromone Annulation of o-Hydroxyaryl Enaminones","volume":"36","author":"Mao","year":"2025","journal-title":"Chin. Chem. Lett."},{"key":"2026103005080997200_cit13g","doi-asserted-by":"publisher","first-page":"404","DOI":"10.1007\/s10593-020-02675-8","article-title":"Recent Advances in Green Synthesis of Chromones","volume":"56","author":"Vavsari","year":"2020","journal-title":"Chem. Heterocycl. Compd."},{"key":"2026103005080997200_cit14a","doi-asserted-by":"publisher","first-page":"1059","DOI":"10.1016\/j.chempr.2019.01.006","article-title":"Recent Advances in the Catalytic Synthesis of 4-Quinolones","volume":"5","author":"Shen","year":"2019","journal-title":"Chem"},{"key":"2026103005080997200_cit14b","doi-asserted-by":"publisher","DOI":"10.1002\/adsc.202500210","article-title":"Recent Advances in the Assembly of Organoselenyl-Substituted (Thio)Chromones and 4-Quinolones","volume":"367","author":"Chen","year":"2025","journal-title":"Adv. Synth. Catal."},{"key":"2026103005080997200_cit14c","doi-asserted-by":"publisher","first-page":"212","DOI":"10.1021\/ol902626d","article-title":"Palladium-Catalyzed Tandem Amination Reaction for the Synthesis of 4-Quinolones","volume":"12","author":"Zhao","year":"2010","journal-title":"Org. Lett."},{"key":"2026103005080997200_cit14d","doi-asserted-by":"publisher","first-page":"8657","DOI":"10.1039\/d3ra00749a","article-title":"Recent Advances in the Synthesis of Pharmaceutically Active 4-Quinolone and Its Analogues: A Review","volume":"13","author":"Dine","year":"2023","journal-title":"RSC Adv."},{"key":"2026103005080997200_cit14e","doi-asserted-by":"publisher","first-page":"4044","DOI":"10.1002\/ejoc.201402224","article-title":"Gold-Catalyzed Conversion of Aryl- and Alkyl-Substituted 1-(o-Aminophenyl)-2-propyn-1-ones to the Corresponding 2-Substituted 4-Quinolones","volume":"2014","author":"Seppanen","year":"2014","journal-title":"Eur. J. Org. Chem."},{"key":"2026103005080997200_cit14f","doi-asserted-by":"publisher","first-page":"3373","DOI":"10.1002\/adsc.201900286","article-title":"Copper-Catalyzed Synthesis of Substituted 4-Quinolones Using Water as a Benign Reaction Media: Application for the Construction of Oxolinic Acid and BQCA","volume":"361","author":"Gore","year":"2019","journal-title":"Adv. Synth. Catal."},{"key":"2026103005080997200_cit14g","doi-asserted-by":"publisher","first-page":"3888","DOI":"10.1039\/d0ob00745e","article-title":"Gold(III)-Catalyzed Azide\u2013Yne Cyclization\/O\u2013H Insertion Cascade Reaction for the Expeditious Construction of 3-Alkoxy-4-Quinolinone Frameworks","volume":"18","author":"Huang","year":"2020","journal-title":"Org. Biomol. Chem."},{"key":"2026103005080997200_cit14h","doi-asserted-by":"publisher","first-page":"1464","DOI":"10.1021\/jo502400h","article-title":"Synthesis of 4-Quinolones via a Carbonylative Sonogashira Cross-Coupling Using Molybdenum Hexacarbonyl as a CO Source","volume":"80","author":"Akerbladh","year":"2015","journal-title":"J. Org. Chem."},{"key":"2026103005080997200_cit14i","doi-asserted-by":"publisher","first-page":"6432","DOI":"10.1021\/acs.orglett.7b03337","article-title":"From Ketones, Amines, and Carbon Monoxide to 4-Quinolones: Palladium-Catalyzed Oxidative Carbonylation","volume":"19","author":"Wu","year":"2017","journal-title":"Org. Lett."},{"key":"2026103005080997200_cit14j","doi-asserted-by":"publisher","first-page":"4984","DOI":"10.1021\/acs.orglett.7b02495","article-title":"Direct Synthesis of 4-Quinolones via Copper-Catalyzed Anilines and Alkynes","volume":"19","author":"Xu","year":"2017","journal-title":"Org. Lett."},{"key":"2026103005080997200_cit15","doi-asserted-by":"publisher","first-page":"644","DOI":"10.1021\/acs.joc.3c02399","article-title":"Photoredox-Catalyzed Tandem Cyclization of Enaminones with N-Sulfonylaminopyridinium Salts Toward the Synthesis of 3-Sulfonaminated Chromones","volume":"89","author":"Hu","year":"2024","journal-title":"J. Org. Chem."},{"key":"2026103005080997200_cit16","doi-asserted-by":"publisher","first-page":"13634","DOI":"10.1021\/acs.joc.3c01339","article-title":"Visible-Light-Induced Synthesis of 3-Alkyl Chromones under Catalyst- and Additive-Free Conditions","volume":"88","author":"Zhao","year":"2023","journal-title":"J. Org. Chem."},{"key":"2026103005080997200_cit17a","doi-asserted-by":"publisher","first-page":"212","DOI":"10.1021\/acs.orglett.4c04209","article-title":"Electrochemical Synthesis of 3-(sulfonyl)quinol-4-ones from o-Alkynyl-N-(formyl)anilides and Sulfinates","volume":"27","author":"Bondarev","year":"2025","journal-title":"Org. Lett."},{"key":"2026103005080997200_cit17b","doi-asserted-by":"publisher","first-page":"12024","DOI":"10.1021\/acs.orglett.5c01981","article-title":"A Cut-and-Sew Strategy with Rongalite: Sulfonylmethylation Relay of Two DistinctAlkenesto Access Lactam-Chromone Hybrid Alkyl-Alkyl Sulfones","volume":"27","author":"Wang","year":"2025","journal-title":"Org.Lett."},{"key":"2026103005080997200_cit18a","doi-asserted-by":"publisher","first-page":"21013","DOI":"10.1039\/D2NJ04021B","article-title":"Recent Advances in Free Radical Cyclizations of 2-Alkenyl Benzaldehydes to Synthesize Benzocycloketones","volume":"46","author":"Chen","year":"2022","journal-title":"New J. Chem."},{"key":"2026103005080997200_cit18b","doi-asserted-by":"publisher","first-page":"539","DOI":"10.1016\/j.ejmech.2015.02.048","article-title":"Recent Advances of Chroman-4-one Derivatives: Synthetic Approaches and Bioactivities","volume":"93","author":"Emami","year":"2015","journal-title":"Eur. J. Med. Chem."},{"key":"2026103005080997200_cit19","doi-asserted-by":"publisher","first-page":"5949","DOI":"10.1016\/j.tetlet.2006.06.064","article-title":"Radical Promoted Cyclizations of Aromatic Carbonyl Compounds to Benzopyrans Using Titanocene(III) Chloride","volume":"47","author":"Jana","year":"2006","journal-title":"Tetrahedron Lett."},{"key":"2026103005080997200_cit20","doi-asserted-by":"publisher","first-page":"12374","DOI":"10.1021\/acs.orglett.5c04023","article-title":"Visible-Light-Promoted Metal-Free Three-Component Reaction for the Synthesis of Sulfonated 4-Amino-chromans, 4-Amino-tetrahydroquinolines, and 5-Amino-dihydrobenzo[b]oxepines","volume":"27","author":"Sheng","year":"2025","journal-title":"Org. Lett."},{"key":"2026103005080997200_cit21a","doi-asserted-by":"publisher","first-page":"10704","DOI":"10.1021\/acs.joc.7b01841","article-title":"Visible-Light Mediated Oxidative C\u2013H\/N\u2013H Cross-Coupling between Tetrahydrofuran and Azoles Using Air","volume":"82","author":"Zhang","year":"2017","journal-title":"J. Org. Chem."},{"key":"2026103005080997200_cit21b","doi-asserted-by":"publisher","first-page":"6564","DOI":"10.1039\/c8ob01922c","article-title":"Synthesis of oxindoles through trifluoromethylation of N-aryl acrylamides by photoredox catalysis","volume":"16","author":"Lu","year":"2018","journal-title":"Org. Biomol. Chem."},{"key":"2026103005080997200_cit21c","doi-asserted-by":"publisher","first-page":"3867","DOI":"10.6023\/cjoc202005018","article-title":"Application of 2,4,5,6-tetrakis(9-carbazolyl)isophthalonitrile as a novel photocatalyst in metal-free organic photosynthesis","volume":"40","author":"Chen","year":"2020","journal-title":"Chin. J. Org. Chem."},{"key":"2026103005080997200_cit21d","doi-asserted-by":"publisher","first-page":"15842","DOI":"10.6023\/cjoc202005018","article-title":"Photoredox-catalyzed sulfonylation of alkenes with sodium benzenesulfinate","volume":"6","author":"Chen","year":"2021","journal-title":"ACS Omega"},{"key":"2026103005080997200_cit21e","doi-asserted-by":"publisher","first-page":"469","DOI":"10.1021\/ar00156a006","article-title":"Electrochemistry of oxygen in nonaqueous solvents","volume":"21","author":"Sawyer","year":"1988","journal-title":"Acc. Chem. Res."},{"key":"2026103005080997200_cit21f","doi-asserted-by":"publisher","first-page":"241","DOI":"10.1016\/j.jelechem.2003.11.026","article-title":"Redox thermodynamics of superoxide\/peroxide couple in aprotic media","volume":"566","author":"Zhang","year":"2004","journal-title":"J. Electroanal. Chem."},{"key":"2026103005080997200_cit22","doi-asserted-by":"publisher","first-page":"9810","DOI":"10.1021\/acs.joc.6b01881","article-title":"Synthesis of allylic amide functionalized 2H-chromenes and coumarins using a one-pot Overman rearrangement and gold(I)-catalyzed hydroarylation","volume":"81","author":"Sharif","year":"2016","journal-title":"J. Org. Chem."},{"key":"2026103005080997200_cit23","doi-asserted-by":"publisher","first-page":"6355","DOI":"10.1039\/C9OB01060B","article-title":"Convenient one-pot access to 2 H-3-nitrothiochromenes from 2-bromobenzaldehydes, sodium sulfide and \u03b2-nitrostyrenes","volume":"17","author":"Le","year":"2019","journal-title":"Org. Biomol. Chem."}],"container-title":["The Journal of Organic Chemistry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.joc.6c01871","content-type":"application\/pdf","content-version":"vor","intended-application":"unspecified"},{"URL":"https:\/\/pubs.acs.org\/joceah\/article-pdf\/91\/43\/14454\/68750953\/jo-2026-01871j.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/pubs.acs.org\/joceah\/article-pdf\/91\/43\/14454\/68750953\/jo-2026-01871j.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,10,30]],"date-time":"2026-10-30T09:30:28Z","timestamp":1793352628000},"score":1,"resource":{"primary":{"URL":"https:\/\/pubs.acs.org\/joceah\/article\/91\/43\/14454\/5444866\/Visible-Light-Induced-Synthesis-for-Sulfonyl-Thio"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,10,5]]},"references-count":55,"journal-issue":{"issue":"43","published-online":{"date-parts":[[2026,10,5]]},"published-print":{"date-parts":[[2026,10,30]]}},"URL":"https:\/\/doi.org\/10.1021\/acs.joc.6c01871","relation":{},"ISSN":["0022-3263","1520-6904"],"issn-type":[{"value":"0022-3263","type":"print"},{"value":"1520-6904","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,10,5]]}}}