Expansion of photocatalytic C(sp3)-H functionalization to allylation, alkynylation, and imination

• 資料種別: 記事
• タイトル: Expansion of photocatalytic C(sp3)-H functionalization to allylation, alkynylation, and imination
• 著者・編者: Yi-Lun Shih; Sheng-Hao Huang; Yen-Ku Wu
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2022-09-08
• 出版年（W3CDTF）: 2022-09-08
• タイトル（掲載誌）: Bulletin of the Chemical Society of Japan
• 巻号年月日等（掲載誌）: 95(10)
• 掲載巻: 95(10)
• ISSN（掲載誌）: 1348-0634
• ISSN-L（掲載誌）: 0009-2673
• 本文の言語コード: eng
• DOI: 10.1246/bcsj.20220171; https://doi.org/10.1246/bcsj.20220171
• 国立国会図書館永続的識別子: info:ndljp/pid/12686458; https://dl.ndl.go.jp/pid/12686458
• コレクション（共通）: 障害者向け資料
• コレクション（障害者向け資料：レベル1）: テキストデータ
• コレクション（個別）: 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会; https://dl.ndl.go.jp/collections/B00043
• 収集根拠: オンライン資料収集制度
• 受理日（W3CDTF）: 2023-03-07T17:43:09+09:00
• 保存日（W3CDTF）: 2023-01-20
• 記録形式（IMT）: application/pdf
• オンライン閲覧公開範囲: 国立国会図書館内限定公開
• デジタル化資料送信: 図書館・個人送信対象外
• 遠隔複写可否（NDL）: 可
• 掲載誌（URI）: https://www.journal.csj.jp/toc/bcsj/95/10
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/12686454; https://dl.ndl.go.jp/pid/12686454
• 連携機関・データベース: 国立国会図書館 : 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp

• 要約等: コレクション : 国立国会図書館デジタルコレクション > 電子書籍・電子雑誌 > 学術機関 > 学協会
• DOI: 10.1246/bcsj.20220171; https://doi.org/10.1246/bcsj.20220171
• オンライン閲覧公開範囲: インターネット公開
• 関連情報（URI）: http://id.ndl.go.jp/digimeta/12686458; https://dl.ndl.go.jp/pid/12686458; https://academic.oup.com/bcsj/article-pdf/95/10/1501/56314392/bcsj.20220171.pdf
• 参照: CO‐Boosted Protocol for the Photocatalytic C−H Thiolation of Aldehydes Using Phenylthiobenzenesulfonate; https://cir.nii.ac.jp/crid/1360306905630480512; 1,2-Bis(phenylsulfonyl)ethylene (BPSE): A Potent Radical C2 Synthon Available in the Radical and Electron-Transfer-Based Organic Synthesis; https://cir.nii.ac.jp/crid/1360025429440648192; Site‐Selective Direct Intermolecular C(<i>sp</i>³)−H Alkylation of Saccharides and Switching of Reaction Sites by Changing Photocatalysts; https://cir.nii.ac.jp/crid/1360865815680358144; Photocatalytic C(sp ³ )–H thiolation by a double S _H 2 strategy using thiosulfonates; https://cir.nii.ac.jp/crid/1360021390581239936
• 参照: Synthesis of Unnatural α-Amino Acid Derivatives via Photoredox Activation of Inert C(sp³)–H Bonds; https://cir.nii.ac.jp/crid/1360579819983671424; Site‐Selective C(<i>sp</i>³)‐H Alkenylation Using Decatungstate Anion as Photocatalyst; https://cir.nii.ac.jp/crid/1360294643758070400; Decatungstate-photocatalysed C(sp³)–H azidation; https://cir.nii.ac.jp/crid/1360579820497669120; Decatungstate Catalyzed Synthesis of Trifluoromethylthioesters from Aldehydes via a Radical Process; https://cir.nii.ac.jp/crid/1360579820402041216; Radical Transformation of Aliphatic C–H Bonds to Oxime Ethers via Hydrogen Atom Transfer; https://cir.nii.ac.jp/crid/1360579819989453440; Direct Photocatalyzed Hydrogen Atom Transfer (HAT) for Aliphatic C–H Bonds Elaboration; https://cir.nii.ac.jp/crid/1360294645881627520; Photoinduced intermolecular hydrogen atom transfer reactions in organic synthesis; https://cir.nii.ac.jp/crid/1360013173250367360; Photocatalytic C–H Trifluoromethylthiolation by the Decatungstate Anion; https://cir.nii.ac.jp/crid/1360576120381432192; Direct C(sp³)–H Cyanation Enabled by a Highly Active Decatungstate Photocatalyst; https://cir.nii.ac.jp/crid/1360013173223083520; Decatungstate-Catalyzed C(<i>sp</i>³)–H Sulfinylation: Rapid Access to Diverse Organosulfur Functionality; https://cir.nii.ac.jp/crid/1360013172318912384; Decatungstate as Direct Hydrogen Atom Transfer Photocatalyst for SOMOphilic Alkynylation; https://cir.nii.ac.jp/crid/1360579818096009984; Site‐Selective Alkenylation of Unactivated C(sp³)−H Bonds Mediated by Compact Sulfate Radical; https://cir.nii.ac.jp/crid/1360294647131462016; Visible Light‐Enabled sp³‐C−H Functionalization with Chloro‐ and Bromoalkynes: Chemoselective Route to Vinylchlorides or Alkynes; https://cir.nii.ac.jp/crid/1360861295057814272; Photochemical Functionalization of Heterocycles with EBX Reagents: C−H Alkynylation versus Deconstructive Ring Cleavage**; https://cir.nii.ac.jp/crid/1360579818111235840; Photocatalytic hydrogen atom transfer: the philosopher's stone for late-stage functionalization?; https://cir.nii.ac.jp/crid/1360576120649835392; Bromine-Radical-Mediated Site-Selective Allylation of C(sp3)–H Bonds; https://cir.nii.ac.jp/crid/1360849943596792064; Catalytic alkylation of unactivated C(sp ³ )–H bonds for C(sp ³ )–C(sp ³ ) bond formation; https://cir.nii.ac.jp/crid/1360011145877020800; Aliphatic C–H Oxidations for Late-Stage Functionalization; https://cir.nii.ac.jp/crid/1363388844654270720; The Quest for Selectivity in Hydrogen Atom Transfer Based Aliphatic C–H Bond Oxygenation; https://cir.nii.ac.jp/crid/1360292621365812864; The hydrogen atom transfer reactivity of sulfinic acids; https://cir.nii.ac.jp/crid/1360855571372811776; α-Arylation of alkylamines with sulfonylarenes through a radical chain mechanism; https://cir.nii.ac.jp/crid/1360848658554912640; Site-Selective C–H Functionalization by Decatungstate Anion Photocatalysis: Synergistic Control by Polar and Steric Effects Expands the Reaction Scope; https://cir.nii.ac.jp/crid/1360283691592106496; Introduction: CH Activation; https://cir.nii.ac.jp/crid/1360855569119159168; Radical C(sp ³ )–H alkenylation, alkynylation and allylation of ethers and amides enabled by photocatalysis; https://cir.nii.ac.jp/crid/1361137044509581056; Aryl Ketone Catalyzed Radical Allylation of C(sp³)–H Bonds under Photoirradiation; https://cir.nii.ac.jp/crid/1363388845639887488; Decatungstate Anion for Photocatalyzed “Window Ledge” Reactions; https://cir.nii.ac.jp/crid/1361981471207310080; Recent Advances in C–H Functionalization; https://cir.nii.ac.jp/crid/1360574096537465088; Evolution of C–H Bond Functionalization from Methane to Methodology; https://cir.nii.ac.jp/crid/1361137045076876800; Photochemically induced radical alkynylation of C(sp ³ )–H bonds; https://cir.nii.ac.jp/crid/1364233269967784704; Radical additions to allyl bromides. A synthetically useful, ‘Tin-Free’ method for carbon–carbon bond formation; https://cir.nii.ac.jp/crid/1362262945335300096; Novel Radical Reaction of Phenylsulfonyl Oxime Ethers. A Free Radical Acylation Approach; https://cir.nii.ac.jp/crid/1361981470536427264; Alkynylation of C−H Bonds via Reaction with Acetylenic Triflones¹; https://cir.nii.ac.jp/crid/1361699994386450176
• 連携機関・データベース: 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• 提供元機関・データベース: 国立国会図書館デジタルコレクション; https://dl.ndl.go.jp; Crossref; https://www.crossref.org; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja