{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1363388844780847744.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1002/anie.201903726"}},{"identifier":{"@type":"URI","@value":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201903726"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201903726"}},{"identifier":{"@type":"URI","@value":"https://onlinelibrary.wiley.com/doi/full-xml/10.1002/anie.201903726"}}],"dc:title":[{"@value":"The Persistent Radical Effect in Organic Synthesis"}],"description":[{"type":"abstract","notation":[{"@value":"<jats:title>Abstract</jats:title><jats:p>Radical–radical couplings are mostly nearly diffusion‐controlled processes. Therefore, the selective cross‐coupling of two different radicals is challenging and not a synthetically valuable transformation. However, if the radicals have different lifetimes and if they are generated at equal rates, cross‐coupling will become the dominant process. This high cross‐selectivity is based on a kinetic phenomenon called the persistent radical effect (PRE). In this Review, an explanation of the PRE supported by simulations of simple model systems is provided. Radical stabilities are discussed within the context of their lifetimes, and various examples of PRE‐mediated radical–radical couplings in synthesis are summarized. It is shown that the PRE is not restricted to the coupling of a persistent with a transient radical. If one coupling partner is longer‐lived than the other transient radical, the PRE operates and high cross‐selectivity is achieved. This important point expands the scope of PRE‐mediated radical chemistry. The Review is divided into two parts, namely 1) the coupling of persistent or longer‐lived organic radicals and 2) “radical–metal crossover reactions”; here, metal‐centered radical species and more generally longer‐lived transition‐metal complexes that are able to react with radicals are discussed—a field that has flourished recently.</jats:p>"}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1383388844780847744","@type":"Researcher","foaf:name":[{"@value":"Dirk Leifert"}],"jpcoar:affiliationName":[{"@value":"Organisch-Chemisches Institut Westfälische Wilhelms-Universität  Corrensstraße 40 48149 Münster Germany"}]},{"@id":"https://cir.nii.ac.jp/crid/1383388844780847745","@type":"Researcher","foaf:name":[{"@value":"Armido Studer"}],"jpcoar:affiliationName":[{"@value":"Key Laboratory of Coal to Ethylene Glycol and Its Related Technology State Key Laboratory of Structural Chemistry Center for Excellence in Molecular Synthesis Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences  155 Yangqiao Road West Fuzhou Fujian 350002 P. R. China"},{"@value":"Organisch-Chemisches Institut Westfälische Wilhelms-Universität  Corrensstraße 40 48149 Münster Germany"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"14337851"},{"@type":"EISSN","@value":"15213773"}],"prism:publicationName":[{"@value":"Angewandte Chemie International Edition"}],"dc:publisher":[{"@value":"Wiley"}],"prism:publicationDate":"2019-10-31","prism:volume":"59","prism:number":"1","prism:startingPage":"74","prism:endingPage":"108"},"reviewed":"false","dc:rights":["http://onlinelibrary.wiley.com/termsAndConditions#vor"],"url":[{"@id":"https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fanie.201903726"},{"@id":"https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201903726"},{"@id":"https://onlinelibrary.wiley.com/doi/full-xml/10.1002/anie.201903726"}],"createdAt":"2019-05-22","modifiedAt":"2023-09-05","relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1050024725022119936","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Organic Photoredox-Catalyzed Silyl Radical Generation from Silylboronate"}]},{"@id":"https://cir.nii.ac.jp/crid/1050292162810158976","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Organophotoredox-catalyzed semipinacol rearrangement via radical-polar crossover"}]},{"@id":"https://cir.nii.ac.jp/crid/1050306199998818816","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Diastereoselective congested β-amido ketone synthesis via NHC-catalyzed radical-radical coupling"}]},{"@id":"https://cir.nii.ac.jp/crid/1050587981427505408","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Visible-Light-Driven α-Allylation of Carboxylic Acids"}]},{"@id":"https://cir.nii.ac.jp/crid/1050866882759094272","@type":"Article","resourceType":"記事(article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Distal C–H functionalization of alkoxyarenes through organic photoredox-catalyzed radical–radical coupling"}]},{"@id":"https://cir.nii.ac.jp/crid/1360009142632790400","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Direct Synthesis of Dialkyl Ketones from Aliphatic Aldehydes through Radical <i>N</i>-Heterocyclic Carbene Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360017279824016640","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Pd‐catalyzed Aerobic Cross‐Dehydrogenative Coupling of Catechols with 2‐Oxindoles and Benzofuranones: Reactivity Difference Between Monomer and Dimer"}]},{"@id":"https://cir.nii.ac.jp/crid/1360017288294641536","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Photoinduced Specific Acylation of Phenolic Hydroxy Groups with Aldehydes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360025431102354816","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Catalytic Aerobic Carbooxygenation for the Construction of Vicinal Tetrasubstituted Centers: Application to the Synthesis of Hexasubstituted γ‐Lactones"}]},{"@id":"https://cir.nii.ac.jp/crid/1360286993070363264","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Organophotoredox-Catalyzed Decarboxylative C(sp<sup>3</sup>)–O Bond Formation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360290493084995072","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Photoinduced Direct Addition of Alkylarenes to Imines"}]},{"@id":"https://cir.nii.ac.jp/crid/1360290617684142464","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Pd/light-induced alkyl–alkenyl coupling reaction between unactivated alkyl iodides and alkenylboronic acids"}]},{"@id":"https://cir.nii.ac.jp/crid/1360290617725395840","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Regiodivergent Oxidative Cross-Coupling of Catechols with Persistent <i>tert</i>-Carbon Radicals"}]},{"@id":"https://cir.nii.ac.jp/crid/1360290617742485120","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Recent advances in N-heterocyclic carbene-based radical catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360294643849000192","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Highly Selective Monoalkylation of Active Methylene and Related Derivatives using Alkylsilyl Peroxides by a Catalytic CuI‐DMAP System"}]},{"@id":"https://cir.nii.ac.jp/crid/1360302866830418304","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A Quadruple Catalysis Enabling Intermolecular Branch‐Selective Hydroacylation of Styrenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360302869448979200","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Diverse Metastable Diarylacetonitrile Radicals Generated by Polymer Mechanochemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1360306905608307712","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Catalytic Reductive Homocoupling of Benzyl Chlorides Enabled by Zirconocene and Photoredox Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360306906073321600","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Use of Aliphatic Carboxylic Acid Derivatives for NHC/Photoredox-Catalyzed meta-Selective Acylation of Electron-Rich Arenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360568468044140032","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Generation of Alkyl Radical through Direct Excitation of Boracene-Based Alkylborate"}]},{"@id":"https://cir.nii.ac.jp/crid/1360572092586203904","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"N-Heterocyclic Carbene-Based Catalysis Enabling Cross-Coupling Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360576118754315392","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A Photocatalytic System Composed of Benzimidazolium Aryloxide and Tetramethylpiperidine 1-Oxyl to Promote Desulfonylative α-Oxyamination Reactions of α-Sulfonylketones"}]},{"@id":"https://cir.nii.ac.jp/crid/1360581630976213504","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"N-heterocyclic carbene- and organic photoredox-catalysed meta-selective acylation of electron-rich arenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360584339764839040","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Fe-Catalyzed Dicarbofunctionalization of Vinylarenes with Alkylsilyl Peroxides and β-Keto Carbonyl Substrates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360584340513293440","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Catalytic oxidative carbon–carbon bond-formations of benzene-1,2-diols"}]},{"@id":"https://cir.nii.ac.jp/crid/1360584341822878336","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of 1,3‑dicarbonyl compounds bearing hetero-substituted α-quaternary carbon via Fe(II)-catalyzed alkylation with alkylsilyl peroxides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360584341823140096","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Fe-Catalyzed Three-Component Coupling Reaction of α,β,γ,δ-Unsaturated Carbonyl Compounds and Conjugate Dienes with Alkylsilyl Peroxides and Nucleophiles"}]},{"@id":"https://cir.nii.ac.jp/crid/1360588379364610688","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"NHC-Mediated Radical Acylation Catalyzed by Thiamine- and Flavin-Dependent Enzymes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360588381069993344","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"α‐Halocarbonyls as a Valuable Functionalized Tertiary Alkyl Source"}]},{"@id":"https://cir.nii.ac.jp/crid/1360588381075829632","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Thiobenzoic Acid-Catalyzed Cα–H Cross Coupling of Benzyl Alcohols with α-Ketoacid Derivatives"}]},{"@id":"https://cir.nii.ac.jp/crid/1360853567816898304","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Non-symmetric mechanophores prepared from radical-type symmetric mechanophores: bespoke mechanofunctional polymers"}]},{"@id":"https://cir.nii.ac.jp/crid/1360857593651794688","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Sterically Hindered α-Hydroxycarbonyls through Radical–Radical Coupling"}]},{"@id":"https://cir.nii.ac.jp/crid/1360857593654497920","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Radical Relay Trichloromethylacylation of Alkenes through N-Heterocyclic Carbene Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360857593654526848","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Light-Driven <i>N</i>-Heterocyclic Carbene Catalysis Using Alkylborates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360865815488197504","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthetic utility of functionalized alkylsilyl peroxides for Fe-catalyzed and visible-light-promoted radical transformation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360865815498191232","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Redox: Organic Robust Radicals and Their Polymers for Energy Conversion/Storage Devices"}]},{"@id":"https://cir.nii.ac.jp/crid/1360869854343124608","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Et<sub>3</sub>Al/Light-Promoted Radical-Polar Crossover Reactions of α-Alkoxyacyl Tellurides"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233270542137088","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Direct excitation strategy for radical generation in organic synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1390003825209736704","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Formal Aerobic Oxidative Cross-Coupling of Benzofuranones with Azo Compounds Using Pd-μ-hydroxo Complex"}]},{"@id":"https://cir.nii.ac.jp/crid/1390008531554410240","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Carbocation Generation by Organophotoredox Catalysis"}]},{"@id":"https://cir.nii.ac.jp/crid/1390018230027336448","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Radical Chemistry of Photoexcitable Borates"},{"@language":"ja","@value":"光励起ホウ素アート錯体によるラジカル化学の開拓"}]},{"@id":"https://cir.nii.ac.jp/crid/2051151842057848064","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"C-H activation catalyzed by Earth-abundant metals"}]},{"@id":"https://cir.nii.ac.jp/crid/2051151842057855232","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Cross-coupling reactions of persistent tertiary carbon radicals"}]},{"@id":"https://cir.nii.ac.jp/crid/2051714792015490688","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Pd-mediated light-controlled living radical polymerization of methyl acrylate"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1002/anie.201903726"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20200349_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acscatal.0c02849_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acscatal.1c02558_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1002/asia.202200807_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1016/j.checat.2023.100736_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1002/anie.202405876_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/jacs.9b12335_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20200376_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1246/cl.210478_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1039/d0qo00318b_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acscatal.0c03986_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1039/d0sc01538e_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1002/ajoc.202100440_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acscatal.2c01964_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1038/s41467-022-30395-4_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1002/chem.202301484_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1038/s44160-023-00378-4_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/prechem.4c00077_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1039/d4sc08407a_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1055/a-2281-2975_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1248/cpb.c20-00359_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.79.1005_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acscatal.0c01795_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acsomega.1c06857_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.2c00656_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1515/pac-2023-0706_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1016/j.tetlet.2022.154176_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.2c00885_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/jacs.5c04484_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1002/open.202400108_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.4c01594_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/jacs.0c04456_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1039/d0cc08048a_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1002/anie.202008897_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.1c01358_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.1c02639_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acscatal.1c04153_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1039/d1cs00262g_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1246/bcsj.20220230_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.82.367_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1039/d3sc06857a_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acs.chemrev.3c00172_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1039/d3mr00031a_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.4c01445_references_DOI_3afxhCHy8BbClHftN3WA4l89nwx"}]}