{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,2]],"date-time":"2026-09-02T05:18:29Z","timestamp":1788326309178,"version":"build-2803163510"},"reference-count":66,"publisher":"American Chemical Society (ACS)","issue":"34","license":[{"start":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T00:00:00Z","timestamp":1786579200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-029"},{"start":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T00:00:00Z","timestamp":1786579200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-037"},{"start":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T00:00:00Z","timestamp":1786579200000},"content-version":"stm-asf","delay-in-days":0,"URL":"https:\/\/doi.org\/10.15223\/policy-045"}],"funder":[{"DOI":"10.13039\/na","name":"University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province","doi-asserted-by":"publisher","award":["UNPYSCT-2017124"],"award-info":[{"award-number":["UNPYSCT-2017124"]}],"id":[{"id":"10.13039\/na","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2026,8,28]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Herein, we report a palladium-catalyzed domino arylation\/dehydrogenative aromatization of acylcyclohexenes to synthesize meta-aryl acetophenone derivatives. This strategy achieves a previously elusive formal meta-C\u2013H arylation of ketones, even with heteroaryl halides. It allows the late-stage introduction of fluorophores and supramolecular motifs, and the robustness is demonstrated by converting biaryl compounds to cumulenes and an AIE fluorescent Na+ probe. Mechanistic investigations revealed a radical process involving an aryl radical as a hydrogen atom transfer reagent.<\/jats:p>","DOI":"10.1021\/acs.orglett.6c02773","type":"journal-article","created":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T08:01:52Z","timestamp":1786608112000},"page":"10719-10724","source":"Crossref","is-referenced-by-count":0,"title":["Construction\nof\n                    <i>meta<\/i>\n                    -Aryl Acetophenone\nDerivatives via Pd-Catalyzed Arylation\/Dehydrogenative Aromatization"],"prefix":"10.1021","volume":"28","author":[{"given":"Jiahui","family":"Ma","sequence":"first","affiliation":[{"name":"Heilongjiang University , , , ,","place":["Harbin, China, 150080"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Qiaoliang","family":"Xu","sequence":"additional","affiliation":[{"name":"Heilongjiang University , , , ,","place":["Harbin, China, 150080"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yaohang","family":"Cheng","sequence":"additional","affiliation":[{"name":"Guizhou Normal University , , ,","place":["Guiyang, China, 550001"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Chenwei","family":"Liang","sequence":"additional","affiliation":[{"name":"Heilongjiang University , , , ,","place":["Harbin, China, 150080"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Siqi","family":"Huang","sequence":"additional","affiliation":[{"name":"Heilongjiang University , , , ,","place":["Harbin, China, 150080"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Guangming","family":"Li","sequence":"additional","affiliation":[{"name":"Heilongjiang University , , , ,","place":["Harbin, China, 150080"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4058-240X","authenticated-orcid":true,"given":"Haoyang","family":"Wang","sequence":"additional","affiliation":[{"name":"Chinese Academy of Sciences , , ,","place":["Shanghai, China, 200032"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jie","family":"Li","sequence":"additional","affiliation":[{"name":"Shanghai Institute of Measurement and Testing Technology Co., Ltd. , ,","place":["Shanghai, China, 201203"]}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3437-5834","authenticated-orcid":true,"given":"Guanghui","family":"An","sequence":"additional","affiliation":[{"name":"Heilongjiang University , , , ,","place":["Harbin, China, 150080"]}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"316","published-online":{"date-parts":[[2026,8,13]]},"reference":[{"key":"2026090200201330100_cit1","doi-asserted-by":"publisher","first-page":"1359","DOI":"10.1021\/cr000664r","article-title":"Aryl\u2013Aryl\nBond Formation One Century after the Discovery of the Ullmann Reaction","volume":"102","author":"Hassan","year":"2002","journal-title":"Chem. Rev."},{"key":"2026090200201330100_cit2","first-page":"299","article-title":"Biaryl Synthesis\nvia C\u2013H Bond Activation: Strategies and Methods","volume-title":"Advances in Organometallic Chemistry","author":"Simonetti","year":"2017"},{"key":"2026090200201330100_cit3","doi-asserted-by":"publisher","first-page":"1461","DOI":"10.1021\/ar800036s","article-title":"Palladium-Catalyzed\nSuzuki\u2013Miyaura Cross-Coupling\nReactions Employing Dialkylbiaryl Phosphine Ligands","volume":"41","author":"Martin","year":"2008","journal-title":"Acc. Chem. Res."},{"key":"2026090200201330100_cit4","doi-asserted-by":"publisher","first-page":"67","DOI":"10.1186\/s43094-023-00520-1","article-title":"Suzuki\u2013Miyaura Cross-Couplings\nfor Alkyl Boron Reagent: Recent Developments\u2500A Review","volume":"9","author":"Ahmed","year":"2023","journal-title":"Futur. J. Pharm. Sci."},{"key":"2026090200201330100_cit5","doi-asserted-by":"publisher","first-page":"351","DOI":"10.35652\/IGJPS.2012.41","article-title":"Suzuki Cross Coupling\nReaction- A Review","volume":"2","author":"Gujral","year":"2012","journal-title":"Indo Global J. Pharm. Sci."},{"key":"2026090200201330100_cit6","doi-asserted-by":"publisher","first-page":"9633","DOI":"10.1016\/S0040-4020(02)01188-2","article-title":"Recent applications\nof the Suzuki\u2013Miyaura\ncross-coupling reaction in organic synthesis","volume":"58","author":"Kotha","year":"2002","journal-title":"Tetrahedron"},{"key":"2026090200201330100_cit7","doi-asserted-by":"publisher","first-page":"1186","DOI":"10.1039\/D0CY02059A","article-title":"Suzuki\u2013Miyaura\ncross coupling reaction: recent advancements in catalysis and organic\nsynthesis","volume":"11","author":"Kadu","year":"2021","journal-title":"Catal. Sci. Technol."},{"key":"2026090200201330100_cit8","doi-asserted-by":"publisher","first-page":"13481","DOI":"10.1002\/chem.202101880","article-title":"Mechanistic\naspects of the palladium-catalyzed\nSuzuki\u2013Miyaura cross-coupling reaction","volume":"27","author":"D\u2019Alterio","year":"2021","journal-title":"Chem.\u2500Eur. J."},{"key":"2026090200201330100_cit9","doi-asserted-by":"publisher","first-page":"381","DOI":"10.1039\/C8GC02860E","article-title":"Recent advances\nin the Suzuki\u2013Miyaura cross-coupling reaction using efficient\ncatalysts in eco-friendly media","volume":"21","author":"Hooshmand","year":"2019","journal-title":"Green Chem."},{"key":"2026090200201330100_cit10","doi-asserted-by":"publisher","first-page":"116124","DOI":"10.1016\/j.poly.2022.116124","article-title":"A retrospective\u2013prospective\nreview of Suzuki\u2013Miyaura reaction: From cross-coupling reaction\nto pharmaceutical industry applications","volume":"227","author":"Farhang","year":"2022","journal-title":"Polyhedron"},{"key":"2026090200201330100_cit11","doi-asserted-by":"publisher","first-page":"7692","DOI":"10.1021\/acs.chemrev.2c00888","article-title":"Transition-Metal-Catalyzed\nC\u2013H\nBond Activation for the Formation of C\u2013C Bonds in Complex Molecules","volume":"123","author":"Docherty","year":"2023","journal-title":"Chem. Rev."},{"key":"2026090200201330100_cit12","doi-asserted-by":"publisher","first-page":"1085","DOI":"10.1038\/s41467-022-28707-9","article-title":"Traditional\nand sustainable\napproaches for the construction of C\u2013C bonds by harnessing\nC\u2013H arylation","volume":"13","author":"Grover","year":"2022","journal-title":"Nat. Commun."},{"key":"2026090200201330100_cit13","doi-asserted-by":"publisher","first-page":"174","DOI":"10.1021\/cr0509760","article-title":"Aryl\u2013Aryl\nBond Formation by\nTransition-Metal-Catalyzed Direct Arylation","volume":"107","author":"Alberico","year":"2007","journal-title":"Chem. Rev."},{"key":"2026090200201330100_cit14","doi-asserted-by":"publisher","first-page":"2447","DOI":"10.1039\/b805701j","article-title":"Recent\nadvances in aryl\u2013aryl bond formation\nby direct arylation","volume":"38","author":"McGlacken","year":"2009","journal-title":"Chem. Soc. Rev."},{"key":"2026090200201330100_cit15","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1002\/9783527627325.ch1","article-title":"Arylation Reactions:\nA Historical Perspective","volume-title":"Modern Arylation\nMethods","author":"Ackermann","year":"2009"},{"key":"2026090200201330100_cit16","doi-asserted-by":"crossref","first-page":"221","DOI":"10.1002\/9783527627325.ch7","article-title":"Palladium-Catalyzed\nArylation Reactions of Alkenes (Mizoroki\u2013Heck Reaction and\nRelated Processes)","volume-title":"Modern Arylation Methods","author":"Trepohl","year":"2009"},{"key":"2026090200201330100_cit17","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1002\/9783527627325.ch10","article-title":"Palladium-Catalyzed\nDirect\nArylation Reactions","volume-title":"Modern Arylation Methods","author":"Miura","year":"2009"},{"key":"2026090200201330100_cit18","doi-asserted-by":"publisher","first-page":"1074","DOI":"10.1021\/ar9000058","article-title":"Palladium-\nand Copper-Catalyzed Arylation\nof Carbon\u2013Hydrogen Bonds","volume":"42","author":"Daugulis","year":"2009","journal-title":"Acc. Chem.\nRes."},{"key":"2026090200201330100_cit19","doi-asserted-by":"publisher","first-page":"1150","DOI":"10.1039\/C8CS00453F","article-title":"Biaryl Synthesis with\nArenediazonium Salts: Cross-Coupling,\nCH-Arylation and Annulation Reactions","volume":"48","author":"Felpin","year":"2019","journal-title":"Chem.\nSoc. Rev."},{"key":"2026090200201330100_cit20","doi-asserted-by":"publisher","first-page":"1082","DOI":"10.1021\/cr9000836","article-title":"Transition Metal-Catalyzed\nDirect Arylation of Substrates with Activated\nsp3-Hybridized C\u2013H Bonds and Some of Their Synthetic\nEquivalents with Aryl Halides and Pseudohalides","volume":"110","author":"Bellina","year":"2010","journal-title":"Chem. Rev."},{"key":"2026090200201330100_cit21","doi-asserted-by":"publisher","first-page":"1","DOI":"10.1055\/a-1939-7052","article-title":"Recent Advances in Room-Temperature\nDirect C\u2013H Arylation Methodologies","volume":"55","author":"Yadav","year":"2023","journal-title":"Synthesis"},{"key":"2026090200201330100_cit22","doi-asserted-by":"publisher","first-page":"6706","DOI":"10.1021\/acs.chemrev.8b00233","article-title":"Electrochemical\nArylation Reaction","volume":"118","author":"Waldvogel","year":"2018","journal-title":"Chem. Rev."},{"key":"2026090200201330100_cit23","doi-asserted-by":"publisher","first-page":"548","DOI":"10.1246\/bcsj.81.548","article-title":"Palladium-Catalyzed\nCH Arylation and Dehydrogenative Homocoupling\nof Heteroaromatic Compounds and Application to the Design of Advanced\nOrganic Materials","volume":"81","author":"Mori","year":"2008","journal-title":"Bull. Chem. Soc. Jpn."},{"key":"2026090200201330100_cit24","doi-asserted-by":"publisher","first-page":"7161","DOI":"10.1002\/anie.201703369","article-title":"A Modular\nFlow Design for the meta-Selective C\u2013H Arylation of Anilines","volume":"56","author":"Gemoets","year":"2017","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit25","doi-asserted-by":"publisher","first-page":"1297","DOI":"10.1039\/C4CC07997C","article-title":"Palladium(II)-Catalyzed meta-Selective\nDirect Arylation of O-\u03b2-Naphthyl Carbamate","volume":"51","author":"Zhang","year":"2015","journal-title":"Chem. Commun."},{"key":"2026090200201330100_cit26","doi-asserted-by":"publisher","first-page":"7668","DOI":"10.1021\/ja201425e","article-title":"Mechanistic Understanding\nof the Unexpected meta Selectivity in Copper-Catalyzed Anilide C\u2013H\nBond Arylation","volume":"133","author":"Chen","year":"2011","journal-title":"J. Am. Chem. Soc."},{"key":"2026090200201330100_cit27","doi-asserted-by":"publisher","first-page":"463","DOI":"10.1002\/anie.201004704","article-title":"Copper(II)-Catalyzed\nmeta-Selective Direct Arylation of \u03b1-Aryl Carbonyl Compounds","volume":"50","author":"Duong","year":"2011","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit28","doi-asserted-by":"publisher","first-page":"347","DOI":"10.1002\/asia.201500506","article-title":"A Domino Oxidation\/Arylation\/Protodecarboxylation\nReaction of Salicylaldehydes: Expanded Access to meta-Arylphenols","volume":"11","author":"Luo","year":"2016","journal-title":"Chem.\u2500Asian J."},{"key":"2026090200201330100_cit29","doi-asserted-by":"publisher","first-page":"7133","DOI":"10.1039\/C8SC02417K","article-title":"meta-C\u2013H Arylation of Fluoroarenes\nvia Traceless Directing Group Relay Strategy","volume":"9","author":"Font","year":"2018","journal-title":"Chem. Sci."},{"key":"2026090200201330100_cit30","doi-asserted-by":"publisher","first-page":"9429","DOI":"10.1002\/anie.201103720","article-title":"Carboxylic\nAcids as Traceless Directing\nGroups for Formal meta-Selective Direct Arylation","volume":"50","author":"Cornella","year":"2011","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit31","doi-asserted-by":"publisher","first-page":"4109","DOI":"10.1021\/ja500457s","article-title":"Overriding Ortho\u2013Para Selectivity\nvia a Traceless Directing Group Relay Strategy: The Meta-Selective\nArylation of Phenols","volume":"136","author":"Luo","year":"2014","journal-title":"J. Am. Chem. Soc."},{"key":"2026090200201330100_cit32","doi-asserted-by":"publisher","first-page":"3127","DOI":"10.1039\/C4CC09674F","article-title":"Salicylic\nAcids as Readily Available\nStarting Materials for the Synthesis of meta-Substituted Biaryls","volume":"51","author":"Luo","year":"2015","journal-title":"Chem. Commun."},{"key":"2026090200201330100_cit33","doi-asserted-by":"publisher","DOI":"10.1002\/advs.202519731","article-title":"A Generalized Approach for Distal\nC\u2013H Arylation of Organic Building Blocks: Unveiling the Role\nof Counter Anion","volume":"13","author":"Grover","year":"2026","journal-title":"Adv. Sci."},{"key":"2026090200201330100_cit34","doi-asserted-by":"publisher","first-page":"7084","DOI":"10.1039\/D3CC01050C","article-title":"Functionalization\nof Arylacetic Acids\nvia Directing-Group-Assisted Remote meta-C\u2013H Activation","volume":"59","author":"Srinivas","year":"2023","journal-title":"Chem. Commun."},{"key":"2026090200201330100_cit35","doi-asserted-by":"publisher","first-page":"3112","DOI":"10.1021\/acs.orglett.5c05320","article-title":"Palladium-Catalyzed Intramolecular meta-C\u2013H\nArylation Assisted by Nitrile Templates Under Microwave-Accelerated\nConditions Accessing Fluorene Frameworks","volume":"28","author":"Mounika","year":"2026","journal-title":"Org.\nLett."},{"key":"2026090200201330100_cit36","doi-asserted-by":"publisher","first-page":"6599","DOI":"10.1021\/acs.orglett.5c01524","article-title":"An Oxidative\nPalladium-Catalyzed Remote meta-Selective Homo-Biaryl Coupling Assisted\nby Nitrile Directing Templates","volume":"27","author":"Sreenivasulu","year":"2025","journal-title":"Org. Lett."},{"key":"2026090200201330100_cit37","doi-asserted-by":"publisher","DOI":"10.1002\/anie.202419954","article-title":"Rhodium-Catalyzed Meta-C\u2013H\nArylation of Arenes with Varied\nLinker Lengths: Bridging Catalytic Selectivity with Structural Diversity","volume":"64","author":"Mandal","year":"2025","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit38","doi-asserted-by":"publisher","first-page":"18056","DOI":"10.1021\/ja410760f","article-title":"Cross-Coupling of\nRemote meta-C\u2013H Bonds Directed by a U-Shaped Template","volume":"135","author":"Wan","year":"2013","journal-title":"J. Am. Chem. Soc."},{"key":"2026090200201330100_cit39","doi-asserted-by":"publisher","first-page":"7279","DOI":"10.1021\/acs.joc.5c00409","article-title":"Access to\nUnsymmetric m-Terphenyl Derivatives via Ligand-Promoted\nPd-Catalyzed Remote meta-C\u2013H Arylation","volume":"90","author":"Yang","year":"2025","journal-title":"J. Org. Chem."},{"key":"2026090200201330100_cit40","doi-asserted-by":"publisher","first-page":"5887","DOI":"10.1021\/jacs.5b02809","article-title":"Simple Amine-Directed Meta-Selective\nC\u2013H Arylation via Pd\/Norbornene Catalysis","volume":"137","author":"Dong","year":"2015","journal-title":"J. Am. Chem. Soc."},{"key":"2026090200201330100_cit41","doi-asserted-by":"publisher","first-page":"11574","DOI":"10.1021\/jacs.5b08914","article-title":"Ligand-Enabled\nMeta-C\u2013H Alkylation and Arylation Using a Modified Norbornene","volume":"137","author":"Shen","year":"2015","journal-title":"J. Am. Chem. Soc."},{"key":"2026090200201330100_cit42","doi-asserted-by":"publisher","first-page":"334","DOI":"10.1038\/nature14214","article-title":"Ligand-Enabled meta-C\u2013H Activation\nUsing a Transient Mediator","volume":"519","author":"Wang","year":"2015","journal-title":"Nature"},{"key":"2026090200201330100_cit43","doi-asserted-by":"publisher","first-page":"9269","DOI":"10.1021\/jacs.6b04966","article-title":"Ligand-Promoted\nMeta-C\u2013H Arylation\nof Anilines, Phenols, and Heterocycles","volume":"138","author":"Wang","year":"2016","journal-title":"J. Am.\nChem. Soc."},{"key":"2026090200201330100_cit44","doi-asserted-by":"publisher","first-page":"417","DOI":"10.1021\/jacs.6b11097","article-title":"Ligand-Enabled\nmeta-Selective C\u2013H Arylation of Nosyl-Protected Phenethylamines,\nBenzylamines, and 2-Aryl Anilines","volume":"139","author":"Ding","year":"2017","journal-title":"J. Am. Chem.\nSoc."},{"key":"2026090200201330100_cit45","doi-asserted-by":"publisher","first-page":"8183","DOI":"10.1002\/anie.201704411","article-title":"meta-C\u2013H Arylation and Alkylation\nof Benzylsulfonamide Enabled by a Palladium(II)\/Isoquinoline Catalyst","volume":"56","author":"Cheng","year":"2017","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit46","doi-asserted-by":"publisher","first-page":"6874","DOI":"10.1002\/anie.201702686","article-title":"Ligand-Enabled Auxiliary-Free\nmeta-C\u2013H Arylation of Phenylacetic Acids","volume":"56","author":"Li","year":"2017","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit47","doi-asserted-by":"publisher","first-page":"5125","DOI":"10.1002\/anie.201701803","article-title":"Ligand-Promoted meta-C\u2013H Functionalization\nof Benzylamines","volume":"56","author":"Wang","year":"2017","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit48","doi-asserted-by":"publisher","first-page":"2166","DOI":"10.1039\/C7CC00110J","article-title":"Palladium-Catalyzed\nInterannular\nmeta-C\u2013H Arylation","volume":"53","author":"Ling","year":"2017","journal-title":"Chem. Commun."},{"key":"2026090200201330100_cit49","doi-asserted-by":"publisher","first-page":"581","DOI":"10.1038\/s41586-018-0220-1","article-title":"Enantioselective\nRemote meta-C\u2013H Arylation and Alkylation via a Chiral Transient\nMediator","volume":"558","author":"Shi","year":"2018","journal-title":"Nature"},{"key":"2026090200201330100_cit50","doi-asserted-by":"publisher","first-page":"7362","DOI":"10.1021\/acscatal.8b01599","article-title":"Palladium-Catalyzed\nmeta-C\u2013H Functionalization of Masked Aromatic Aldehydes","volume":"8","author":"Farmer","year":"2018","journal-title":"ACS Catal."},{"key":"2026090200201330100_cit51","doi-asserted-by":"publisher","first-page":"14870","DOI":"10.1021\/jacs.9b07887","article-title":"meta C\u2013H\nArylation of Electron-Rich Arenes: Reversing the Conventional Site\nSelectivity","volume":"141","author":"Liu","year":"2019","journal-title":"J. Am. Chem. Soc."},{"key":"2026090200201330100_cit52","doi-asserted-by":"publisher","first-page":"13831","DOI":"10.1002\/anie.202002865","article-title":"meta-Selective\nC\u2013H Arylation of Fluoroarenes and Simple Arenes","volume":"59","author":"Liu","year":"2020","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit53","doi-asserted-by":"publisher","DOI":"10.1002\/anie.202201750","article-title":"S,O-Ligand Promoted meta-C\u2013H Arylation of Anisole Derivatives\nvia Palladium\/Norbornene Catalysis","volume":"61","author":"Sukowski","year":"2022","journal-title":"Angew. Chem.,\nInt. Ed."},{"key":"2026090200201330100_cit54","doi-asserted-by":"publisher","DOI":"10.1002\/anie.202317741","article-title":"meta-C\u2013H Arylation of Aniline Derivatives via Palladium\/S,O-Ligand\/Norbornene\nCooperative Catalysis","volume":"63","author":"Sukowski","year":"2024","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit55","doi-asserted-by":"publisher","first-page":"2495","DOI":"10.1021\/acs.orglett.4c00721","article-title":"Native Amino\nGroup Directed Meta-Selective C\u2013H Arylation of Primary Amines\nvia Pd\/Norbornene Catalysis","volume":"26","author":"Zhang","year":"2024","journal-title":"Org. Lett."},{"key":"2026090200201330100_cit56","doi-asserted-by":"publisher","first-page":"15819","DOI":"10.1039\/D4SC03802A","article-title":"meta-C\u2013H\nFunctionalization of Phenylethyl and Benzylic Alcohol Derivatives\nvia Pd\/NBE Relay Catalysis","volume":"15","author":"Shen","year":"2024","journal-title":"Chem. Sci."},{"key":"2026090200201330100_cit57","doi-asserted-by":"publisher","first-page":"6594","DOI":"10.1021\/jacs.4c15491","article-title":"Atroposelective\nDiverse Remote meta-C\u2013H Functionalization\nvia Kinetic Resolution","volume":"147","author":"Li","year":"2025","journal-title":"J. Am. Chem. Soc."},{"key":"2026090200201330100_cit58","doi-asserted-by":"publisher","DOI":"10.1002\/cctc.202301523","article-title":"Visible Light-Induced\nRu-Catalyzed Directing-Group-Assisted\nC\u2013H Activation of Arenes","volume":"16","author":"Wang","year":"2024","journal-title":"ChemCatChem."},{"key":"2026090200201330100_cit59","doi-asserted-by":"publisher","first-page":"108546","DOI":"10.1016\/j.cclet.2023.108546","article-title":"\u03b2-C(sp3)\u2013H Chlorination of Amide Derivatives\nvia Photoinduced Copper\nCharge Transfer Catalysis","volume":"35","author":"He","year":"2024","journal-title":"Chin. Chem. Lett."},{"key":"2026090200201330100_cit60","doi-asserted-by":"publisher","first-page":"122757","DOI":"10.1016\/j.jorganchem.2023.122757","article-title":"Quinoline-Polyoxometalate\nConglomerate as Efficient\nHeterogeneous Catalysts for Visible-Light-Mediated Minisci Reactions","volume":"996","author":"Cai","year":"2023","journal-title":"J. Organomet. Chem."},{"key":"2026090200201330100_cit61","doi-asserted-by":"publisher","first-page":"7310","DOI":"10.1021\/acscatal.3c00901","article-title":"Visible-Light-Mediated Ruthenium-Catalyzed\npara-Selective Alkylation of Unprotected Anilines","volume":"13","author":"Lv","year":"2023","journal-title":"ACS Catal."},{"key":"2026090200201330100_cit62","doi-asserted-by":"publisher","first-page":"2318","DOI":"10.1039\/D2QO01985J","article-title":"Iron-Mediated Divergent\nReductive Coupling Reactions\nof Heteroarenes with Alkenes","volume":"10","author":"Zhang","year":"2023","journal-title":"Org. Chem. Front."},{"key":"2026090200201330100_cit63","doi-asserted-by":"publisher","first-page":"301","DOI":"10.1126\/science.abj4213","article-title":"Univariate\nClassification of Phosphine Ligation State\nand Reactivity in Cross-Coupling Catalysis","volume":"374","author":"Newman-Stonebraker","year":"2021","journal-title":"Science"},{"key":"2026090200201330100_cit64","doi-asserted-by":"publisher","first-page":"23755","DOI":"10.1021\/jacs.3c08290","article-title":"Conjugated [5]Cumulene Polymers Enabled by Condensation Polymerization\nof Propargylic Electrophiles","volume":"145","author":"Wang","year":"2023","journal-title":"J. Am. Chem. Soc."},{"key":"2026090200201330100_cit65","doi-asserted-by":"publisher","first-page":"6645","DOI":"10.1002\/anie.201501810","article-title":"Cumulene Rotaxanes: Stabilization and Study of [9]Cumulenes","volume":"54","author":"Franz","year":"2015","journal-title":"Angew. Chem., Int. Ed."},{"key":"2026090200201330100_cit66","doi-asserted-by":"publisher","first-page":"5561","DOI":"10.1039\/D3QM00679D","article-title":"Recent advances in aggregation-induced emission (AIE)-based chemosensors\nfor the detection of organic small molecules","volume":"7","author":"Chua","year":"2023","journal-title":"Mater. Chem. Front."}],"container-title":["Organic Letters"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.orglett.6c02773","content-type":"application\/pdf","content-version":"vor","intended-application":"unspecified"},{"URL":"https:\/\/pubs.acs.org\/orlef7\/article-pdf\/28\/34\/10719\/66521832\/acs.orglett.6c02773.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"syndication"},{"URL":"https:\/\/pubs.acs.org\/orlef7\/article-pdf\/28\/34\/10719\/66521832\/acs.orglett.6c02773.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2026,9,2]],"date-time":"2026-09-02T04:25:23Z","timestamp":1788323123000},"score":1,"resource":{"primary":{"URL":"https:\/\/pubs.acs.org\/orlef7\/article\/28\/34\/10719\/5254082\/Construction-of-meta-Aryl-Acetophenone-Derivatives"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,8,13]]},"references-count":66,"journal-issue":{"issue":"34","published-online":{"date-parts":[[2026,8,13]]},"published-print":{"date-parts":[[2026,8,28]]}},"URL":"https:\/\/doi.org\/10.1021\/acs.orglett.6c02773","relation":{},"ISSN":["1523-7060","1523-7052"],"issn-type":[{"value":"1523-7060","type":"print"},{"value":"1523-7052","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,8,13]]}}}