{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,4]],"date-time":"2026-09-04T14:23:27Z","timestamp":1788531807051,"version":"build-2803163510"},"reference-count":52,"publisher":"American Chemical Society (ACS)","issue":"35","license":[{"start":{"date-parts":[[2026,8,21]],"date-time":"2026-08-21T00:00:00Z","timestamp":1787270400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2026,8,21]],"date-time":"2026-08-21T00:00:00Z","timestamp":1787270400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2026,8,21]],"date-time":"2026-08-21T00:00:00Z","timestamp":1787270400000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-045"}],"funder":[{"DOI":"10.13039\/501100003787","name":"Natural Science Foundation of Hebei Province","doi-asserted-by":"publisher","award":["B2025201101"],"award-info":[{"award-number":["B2025201101"]}],"id":[{"id":"10.13039\/501100003787","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100008047","name":"Hebei University","doi-asserted-by":"publisher","award":["IT2023B01"],"award-info":[{"award-number":["IT2023B01"]}],"id":[{"id":"10.13039\/501100008047","id-type":"DOI","asserted-by":"publisher"}]},{"name":"Hebei Province Innovation Capability Enhancement Plan","award":["22567632H"],"award-info":[{"award-number":["22567632H"]}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,9,4]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>This study reports a simple and efficient photocatalytic radical cascade cyclization strategy for the one-step synthesis of allyl- and vinyl-sulfonyl fluorides bearing dibenzazepine or dioxodibenzothiazepine scaffolds. In contrast to the existing synthesis methods of allyl sulfonyl fluoride, this approach employs aryl-terminal alkynes as starting materials, thereby avoiding the reliance on preformed allylic frameworks. The reaction utilizes inexpensive and readily accessible \u2013CH2SO2F and \u2013SO2F precursors, exhibits a broad substrate scope, proceeds under mild conditions, and delivers high stereoselectivity. The synthetic utility of this methodology was further demonstrated through SuFEx-based ligation with other molecules.<\/jats:p>","DOI":"10.1021\/acs.joc.6c01229","type":"journal-article","created":{"date-parts":[[2026,8,23]],"date-time":"2026-08-23T17:15:33Z","timestamp":1787505333000},"page":"12016-12022","source":"Crossref","is-referenced-by-count":0,"title":["Photocatalytic Fluorosulfonylmethylation\/Fluorosulfonylation\nof 2-Amino Aryl Ethynes to Access Dibenzazepine-\/Dioxodibenzothiazepine-Functionalized\nAllyl\/Vinyl Sulfonyl Fluorides"],"prefix":"10.1021","volume":"91","author":[{"given":"Jian-Hong","family":"Zhang","sequence":"first","affiliation":[{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yun-Qi","family":"Lin","sequence":"additional","affiliation":[{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ye-Pu","family":"Fu","sequence":"additional","affiliation":[{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yan-Hui","family":"Li","sequence":"additional","affiliation":[{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jun-Zhao","family":"Ma","sequence":"additional","affiliation":[{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lele","family":"Zhang","sequence":"additional","affiliation":[{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-5069-5945","authenticated-orcid":true,"given":"Wei","family":"Li","sequence":"additional","affiliation":[{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]},{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-2411-2758","authenticated-orcid":true,"given":"Li-Jing","family":"Wang","sequence":"additional","affiliation":[{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]},{"name":"Hebei University , , ,","place":["Baoding, P. R. China, 071002"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"316","published-online":{"date-parts":[[2026,8,21]]},"reference":[{"key":"2026090408100100600_cit1a","doi-asserted-by":"publisher","first-page":"9430","DOI":"10.1002\/anie.201309399","article-title":"Sulfur(VI)\nfluoride exchange (SuFEx): another good reaction for click chemistry","volume":"53","author":"Dong","year":"2014","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090408100100600_cit1b","doi-asserted-by":"publisher","first-page":"2919","DOI":"10.1021\/jacs.7b12788","article-title":"SuFEx Click Chemistry Enabled Late-Stage\nDrug Functionalization","volume":"140","author":"Liu","year":"2018","journal-title":"J. Am. Chem. Soc."},{"key":"2026090408100100600_cit1c","doi-asserted-by":"publisher","first-page":"10899","DOI":"10.1021\/jacs.9b13652","article-title":"Sulfur(VI) Fluoride\nExchange (SuFEx)-Enabled High-Throughput Medicinal Chemistry","volume":"142","author":"Kitamura","year":"2020","journal-title":"J. Am. Chem. Soc."},{"key":"2026090408100100600_cit2a","doi-asserted-by":"publisher","first-page":"8278","DOI":"10.1038\/s41467-023-44029-w","article-title":"Electroreductive\nhydroxy fluorosulfonylation of alkenes","volume":"14","author":"Feng","year":"2023","journal-title":"Nat.\nCommun."},{"key":"2026090408100100600_cit2b","doi-asserted-by":"publisher","first-page":"939","DOI":"10.1038\/s41929-025-01405-7","article-title":"A modular synthesis\nof azetidines from reactive triplet imine intermediates using an intermolecular\naza Paterno-Buchi reaction","volume":"8","author":"Williams","year":"2025","journal-title":"Nat. Catal."},{"key":"2026090408100100600_cit2c","doi-asserted-by":"publisher","first-page":"nwad123","DOI":"10.1093\/nsr\/nwad123","article-title":"Advances in the construction\nof diverse SuFEx linkers","volume":"10","author":"Zeng","year":"2023","journal-title":"Natl. Sci. Rev."},{"key":"2026090408100100600_cit2d","doi-asserted-by":"publisher","DOI":"10.1002\/chem.202300536","article-title":"Linkage Chemistry of S(VI) Fluorides","volume":"29","author":"Zeng","year":"2023","journal-title":"Chem. Eur J."},{"key":"2026090408100100600_cit3a","doi-asserted-by":"publisher","first-page":"963","DOI":"10.1002\/pol.20210126","article-title":"Click chemistry\nstrategies for the accelerated synthesis of functional macromolecules","volume":"59","author":"Geng","year":"2021","journal-title":"J. Polym. Sci."},{"key":"2026090408100100600_cit3b","doi-asserted-by":"publisher","first-page":"16348","DOI":"10.1002\/chem.201602926","article-title":"SuFEx Click:\nNew Materials from SOxF and Silyl Ethers","volume":"22","author":"Yatvin","year":"2016","journal-title":"Chem.\nEur J."},{"key":"2026090408100100600_cit3c","doi-asserted-by":"publisher","first-page":"11969","DOI":"10.1002\/anie.201406964","article-title":"Selective\ninhibition of the immunoproteasome by ligand-induced crosslinking\nof the active site","volume":"53","author":"Dubiella","year":"2014","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090408100100600_cit4a","doi-asserted-by":"publisher","first-page":"1356","DOI":"10.1039\/D2OB01891H","article-title":"Sulfur(VI)\nfluorides as tools in biomolecular and medicinal chemistry","volume":"21","author":"Carneiro","year":"2023","journal-title":"Org. Biomol. Chem."},{"key":"2026090408100100600_cit4b","doi-asserted-by":"publisher","first-page":"755","DOI":"10.1038\/s41586-025-09286-3","article-title":"SuFEx-based antitubercular compound irreversibly inhibits Pks13","volume":"645","author":"Krieger","year":"2025","journal-title":"Nature"},{"key":"2026090408100100600_cit5a","doi-asserted-by":"publisher","first-page":"106227","DOI":"10.1016\/j.bioorg.2022.106227","article-title":"Chemical and biology\nof sulfur fluoride exchange (SuFEx) click chemistry for drug discovery","volume":"130","author":"Wilson Lucas","year":"2023","journal-title":"Bioorg. Chem."},{"key":"2026090408100100600_cit5b","doi-asserted-by":"publisher","first-page":"679","DOI":"10.1016\/j.ejmech.2018.11.017","article-title":"Pharmaceutical and medicinal significance of sulfur\n(S(VI))-Containing motifs for drug discovery: A critical review","volume":"162","author":"Zhao","year":"2019","journal-title":"Eur. J. Med. Chem."},{"key":"2026090408100100600_cit5c","doi-asserted-by":"publisher","first-page":"5673","DOI":"10.1021\/acs.jmedchem.8b01153","article-title":"Emerging and Re-Emerging Warheads\nfor Targeted Covalent Inhibitors: Applications in Medicinal Chemistry\nand Chemical Biology","volume":"62","author":"Gehringer","year":"2019","journal-title":"J. Med. Chem."},{"key":"2026090408100100600_cit5d","doi-asserted-by":"publisher","first-page":"3175","DOI":"10.1002\/cphc.201800997","article-title":"Modification\nof Carbon Fibre Surfaces by Sulfur-Fluoride Exchange Click Chemistry","volume":"19","author":"Randall","year":"2018","journal-title":"ChemPhysChem"},{"key":"2026090408100100600_cit6a","doi-asserted-by":"publisher","first-page":"7397","DOI":"10.1002\/anie.202013976","article-title":"A Broad-Spectrum Catalytic\nAmidation of Sulfonyl Fluorides and Fluorosulfates","volume":"60","author":"Wei","year":"2021","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090408100100600_cit6b","doi-asserted-by":"publisher","first-page":"146","DOI":"10.1038\/s41570-021-00352-8","article-title":"Sulfonyl fluorides\nas targets and substrates in the development of new synthetic methods","volume":"6","author":"Lou","year":"2022","journal-title":"Nat. Rev. Chem."},{"key":"2026090408100100600_cit6c","doi-asserted-by":"publisher","DOI":"10.1002\/anie.202112375","article-title":"Accelerated SuFEx Click Chemistry\nFor Modular Synthesis","volume":"61","author":"Smedley","year":"2022","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090408100100600_cit7a","doi-asserted-by":"publisher","first-page":"5395","DOI":"10.1021\/acs.jmedchem.8b00685","article-title":"Potent\nand Highly Selective Inhibitors of the Proteasome Trypsin-like Site\nby Incorporation of Basic Side Chain Containing Amino Acid Derived\nSulfonyl Fluorides","volume":"61","author":"Artschwager","year":"2018","journal-title":"J. Med. Chem."},{"key":"2026090408100100600_cit7b","doi-asserted-by":"publisher","first-page":"3752","DOI":"10.1038\/s41467-019-11805-6","article-title":"A rapid access to aliphatic sulfonyl fluorides","volume":"10","author":"Xu","year":"2019","journal-title":"Nat. Commun."},{"key":"2026090408100100600_cit8a","doi-asserted-by":"publisher","first-page":"957","DOI":"10.1002\/anie.201806037","article-title":"Arylfluorosulfate-Based\nElectrophiles for Covalent Protein Labeling: A New Addition to the\nArsenal","volume":"58","author":"Martin-Gago","year":"2019","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090408100100600_cit8b","doi-asserted-by":"publisher","first-page":"200","DOI":"10.1021\/jacs.7b08366","article-title":"Inverse Drug Discovery\u2033 Strategy To Identify Proteins That\nAre Targeted by Latent Electrophiles As Exemplified by Aryl Fluorosulfates","volume":"140","author":"Mortenson","year":"2018","journal-title":"J. Am. Chem. Soc."},{"key":"2026090408100100600_cit8c","doi-asserted-by":"publisher","first-page":"85","DOI":"10.1016\/j.cell.2020.05.028","article-title":"Developing Covalent Protein Drugs via Proximity-Enabled\nReactive Therapeutics","volume":"182","author":"Li","year":"2020","journal-title":"Cell"},{"key":"2026090408100100600_cit8d","doi-asserted-by":"publisher","first-page":"3753","DOI":"10.1021\/jacs.0c09306","article-title":"Sulfur\n[(18)F]Fluoride Exchange Click Chemistry Enabled Ultrafast Late-Stage\nRadiosynthesis","volume":"143","author":"Zheng","year":"2021","journal-title":"J. Am. Chem. Soc."},{"issue":"28","key":"2026090408100100600_cit8e","doi-asserted-by":"publisher","DOI":"10.1073\/pnas.2103513118","article-title":"Identification of simple arylfluorosulfates as potent agents against\nresistant bacteria","volume":"118","author":"Zhang","year":"2021","journal-title":"Proc. Natl. Acad. Sci. U.S.A."},{"key":"2026090408100100600_cit9a","doi-asserted-by":"publisher","first-page":"2315","DOI":"10.1021\/cr800309r","article-title":"Evolving Organic Synthesis Fostered by the Pluripotent\nPhenylsulfone Moiety","volume":"109","author":"El-Awa","year":"2009","journal-title":"Chem. Rev."},{"key":"2026090408100100600_cit9b","doi-asserted-by":"publisher","first-page":"2018","DOI":"10.1039\/b911852g","article-title":"Sulfones: new reagents in organocatalysis","volume":"39","author":"Alba","year":"2010","journal-title":"Chem. Soc. Rev."},{"key":"2026090408100100600_cit10a","doi-asserted-by":"publisher","first-page":"499","DOI":"10.1021\/jm0400810","article-title":"Identification of 4-Substituted 1,2,3-Triazoles\nas Novel Oxazolidinone Antibacterial Agents with Reduced Activity\nagainst Monoamine Oxidase A","volume":"48","author":"Reck","year":"2005","journal-title":"J. Med. Chem."},{"key":"2026090408100100600_cit10b","doi-asserted-by":"publisher","first-page":"5131","DOI":"10.1002\/ejoc.201200572","article-title":"Antifungal Diterpene\nAlkaloids from the Caribbean Sponge Agelas citrina: Unified Configurational\nAssignments of Agelasidines and Agelasines","volume":"2012","author":"Stout","year":"2012","journal-title":"Eur. J. Org. Chem."},{"key":"2026090408100100600_cit11","doi-asserted-by":"publisher","first-page":"3618","DOI":"10.1021\/acs.joc.3c02706","article-title":"One-Pot Three-Component Synthesis of Indolyl-4H-chromene-3-sulfonyl\nFluoride: A Class of Important Pharmacophore","volume":"89","author":"Yin","year":"2024","journal-title":"J. Org. Chem."},{"key":"2026090408100100600_cit12","doi-asserted-by":"publisher","first-page":"1523","DOI":"10.1016\/j.tet.2004.11.070","article-title":"One-pot synthesis of\n1-aryl-3-methyl-1,3-dienes using methallyl(trimethyl)silane and aldehydes\nand their low temperature (Z)\u2192(E) isomerization induced by sulfur dioxide","volume":"61","author":"Dubbaka","year":"2005","journal-title":"Tetrahedron"},{"key":"2026090408100100600_cit13a","doi-asserted-by":"publisher","first-page":"19402","DOI":"10.1039\/D2RA03733E","article-title":"A regio- and stereoselective Heck-Matsuda process for\nconstruction of gamma-aryl allylsulfonyl fluorides","volume":"12","author":"Qin","year":"2022","journal-title":"RSC Adv."},{"key":"2026090408100100600_cit13b","doi-asserted-by":"publisher","first-page":"7117","DOI":"10.1039\/D4OB01213E","article-title":"A portal\nto highly valuable indole-functionalized vinyl sulfonyl fluorides\nand allylic sulfonyl fluorides","volume":"22","author":"Huang","year":"2024","journal-title":"Org. Biomol.\nChem."},{"key":"2026090408100100600_cit13c","doi-asserted-by":"publisher","first-page":"5554","DOI":"10.1039\/D5OB00487J","article-title":"A protocol for selective synthesis of thiol-functionalized\nallylic sulfonyl fluorides","volume":"23","author":"Ajisafe","year":"2025","journal-title":"Org. Biomol. Chem."},{"key":"2026090408100100600_cit13d","doi-asserted-by":"publisher","first-page":"2641","DOI":"10.1021\/acs.joc.5c03022","article-title":"Selective Construction of Xanthate-Functionalized\nAllylic Sulfonyl Fluorides via a Three-Component Process","volume":"91","author":"Ajisafe","year":"2026","journal-title":"J. Org. Chem."},{"key":"2026090408100100600_cit14","doi-asserted-by":"publisher","first-page":"4760","DOI":"10.1039\/D4NJ05160B","article-title":"Photoredox-catalyzed\nradical fluorosulfonylation of allyl sulfones","volume":"49","author":"Liang","year":"2025","journal-title":"New J. Chem."},{"key":"2026090408100100600_cit15","doi-asserted-by":"publisher","first-page":"2170","DOI":"10.1021\/acs.orglett.5c00256","article-title":"Electrochemical Radical Fluorosufonylation of Allyl Bromides","volume":"27","author":"Liu","year":"2025","journal-title":"Org. Lett."},{"key":"2026090408100100600_cit16","doi-asserted-by":"publisher","first-page":"1656","DOI":"10.1021\/acs.orglett.5c00015","article-title":"Photoredox-Catalyzed Allylic C-H Fluorosulfonylation\nof Alkenes: Accessing Allyl Sulfonyl Fluorides","volume":"27","author":"Yan","year":"2025","journal-title":"Org. Lett."},{"key":"2026090408100100600_cit17","doi-asserted-by":"publisher","first-page":"22035","DOI":"10.1002\/anie.202109072","article-title":"Introducing A New Class\nof Sulfonyl Fluoride Hubs via Radical Chloro-Fluorosulfonylation of\nAlkynes","volume":"60","author":"Nie","year":"2021","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090408100100600_cit18","doi-asserted-by":"publisher","first-page":"27271","DOI":"10.1002\/anie.202112118","article-title":"Electrochemical Oxo-Fluorosulfonylation of Alkynes under Air: Facile\nAccess to beta-Keto Sulfonyl Fluorides","volume":"60","author":"Chen","year":"2021","journal-title":"Angew.\nChem., Int. Ed."},{"key":"2026090408100100600_cit19","doi-asserted-by":"publisher","DOI":"10.1002\/ange.202207684","article-title":"Radical Hydro-Fluorosulfonylation of Unactivated Alkenes and Alkynes","volume":"134","author":"Wang","year":"2022","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090408100100600_cit20a","doi-asserted-by":"publisher","first-page":"1877","DOI":"10.1021\/jm00160a015","article-title":"Tricyclic epines. Novel (E)- and (Z)-11H-dibenz[b,e]azepines as potential central nervous\nsystem agents. Variation of the basic side chain","volume":"29","author":"Steiner","year":"1986","journal-title":"J. Med. Chem."},{"key":"2026090408100100600_cit20b","doi-asserted-by":"publisher","first-page":"104","DOI":"10.1016\/j.bmcl.2008.11.001","article-title":"11-Phenyl-[b,e]-dibenzazepine\ncompounds: novel antitumor agents","volume":"19","author":"Al-Qawasmeh","year":"2009","journal-title":"Bioorg. Med.\nChem. Lett."},{"key":"2026090408100100600_cit20c","doi-asserted-by":"publisher","first-page":"5465","DOI":"10.1016\/j.bmcl.2007.07.002","article-title":"Design, synthesis and biological\nevaluation of substituted dioxodibenzothiazepines and dibenzocycloheptanes\nas farnesyltransferase inhibitors","volume":"17","author":"Gilleron","year":"2007","journal-title":"Bioorg. Med.\nChem. Lett."},{"key":"2026090408100100600_cit20d","doi-asserted-by":"publisher","first-page":"1509","DOI":"10.3762\/bjoc.11.164","article-title":"The enantioselective\nsynthesis of (S)-(+)-mianserin and (S)-(+)-epinastine","volume":"11","author":"Roszkowski","year":"2015","journal-title":"Beilstein J. Org. Chem."},{"key":"2026090408100100600_cit21a","doi-asserted-by":"publisher","first-page":"8039","DOI":"10.1021\/acs.orglett.5c02385","article-title":"Photocatalytic Fluorosulfonylation\/Fluorosulfonamidation\nof N-Homoallyl Aldehyde Hydrazones to Access FSO2-\/FSO2N-Functionalized Tetrahydropyridazines","volume":"27","author":"Dong","year":"2025","journal-title":"Org. Lett."},{"key":"2026090408100100600_cit21b","doi-asserted-by":"publisher","first-page":"2632","DOI":"10.1021\/acs.orglett.6c00017","article-title":"Photoredox-Enabled\nRadical Ring-Opening Fluorosulfonamidation\/Fluorosulfonylmethylation\nof Methylenecyclobutanols","volume":"28","author":"Li","year":"2026","journal-title":"Org. Lett."},{"key":"2026090408100100600_cit21c","doi-asserted-by":"publisher","first-page":"7051","DOI":"10.1021\/acs.orglett.3c02727","article-title":"Photocatalytic\nC-C Bond Cleavage and Fluorosulfonylation of Strained Cycloalkanols\nfor Carbonyl-Containing Aliphatic Sulfonyl Fluorides","volume":"25","author":"Yan","year":"2023","journal-title":"Org. Lett."},{"key":"2026090408100100600_cit21d","doi-asserted-by":"publisher","first-page":"3910","DOI":"10.1021\/acs.orglett.3c01278","article-title":"Aminofluorosulfonylation\nof beta,gamma-Unsaturated Hydrazones with Sulfur Dioxide and N-Fluorobenzenesulfonimide:\nAccessing Pyrazoline-Functionalized Aliphatic Sulfonyl Fluorides","volume":"25","author":"Yan","year":"2023","journal-title":"Org. Lett."},{"key":"2026090408100100600_cit23a","doi-asserted-by":"publisher","first-page":"12141","DOI":"10.1021\/acs.joc.3c01290","article-title":"Photoinduced Tandem\nCyanomethylation\/Cyclization of Unsaturated Compounds: Access to Cyanomethylated\n7- or 5-Membered N-Heterocycles","volume":"88","author":"Guo","year":"2023","journal-title":"J. Org. Chem."},{"key":"2026090408100100600_cit23b","doi-asserted-by":"publisher","DOI":"10.1002\/ejoc.202400969","article-title":"Photo-Induced Difluoroethylation or Monofluoromethyl\nSulfonylation of 2-Amino Aryl Ethynes to Access Diverse Seven-Membered N-Heterocycles","volume":"27","author":"Tian","year":"2024","journal-title":"Eur. J. Org. Chem."}],"container-title":["The Journal of Organic Chemistry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.joc.6c01229","content-type":"application\/pdf","content-version":"vor","intended-application":"unspecified"},{"URL":"https:\/\/pubs.acs.org\/joceah\/article-pdf\/91\/35\/12016\/67054801\/acs.joc.6c01229.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/pubs.acs.org\/joceah\/article-pdf\/91\/35\/12016\/67054801\/acs.joc.6c01229.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,9,4]],"date-time":"2026-09-04T13:48:18Z","timestamp":1788529698000},"score":1,"resource":{"primary":{"URL":"https:\/\/pubs.acs.org\/joceah\/article\/91\/35\/12016\/5292591\/Photocatalytic-Fluorosulfonylmethylation"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,8,21]]},"references-count":52,"journal-issue":{"issue":"35","published-online":{"date-parts":[[2026,8,21]]},"published-print":{"date-parts":[[2026,9,4]]}},"URL":"https:\/\/doi.org\/10.1021\/acs.joc.6c01229","relation":{},"ISSN":["0022-3263","1520-6904"],"issn-type":[{"value":"0022-3263","type":"print"},{"value":"1520-6904","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,8,21]]}}}