A strained vicinal diol as a reductant for coupling of organyl halides

• 資料種別: 記事
• タイトル: A strained vicinal diol as a reductant for coupling of organyl halides
• 著者・編者: Naoki Ishida; Yusuke Masuda; Fangzhu Sun
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2019-06-06
• 出版年（W3CDTF）: 2019-06-06
• タイトル（掲載誌）: Chemistry letters
• 巻号年月日等（掲載誌）: 48(9)
• 掲載巻: 48(9)
• ISSN（掲載誌）: 1348-0715
• ISSN-L（掲載誌）: 0366-7022
• 本文の言語コード: eng
• DOI: 10.1246/cl.190403; https://doi.org/10.1246/cl.190403
• 国立国会図書館永続的識別子: info:ndljp/pid/11552465; https://dl.ndl.go.jp/pid/11552465
• 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）: 2020-10-07T08:55:27+09:00
• 保存日（W3CDTF）: 2019-08-21
• 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/cl/48/9
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/11552460; https://dl.ndl.go.jp/pid/11552460
• 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/cl.190403; https://doi.org/10.1246/cl.190403
• 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/11552465; https://dl.ndl.go.jp/pid/11552465; http://www.journal.csj.jp/doi/pdf/10.1246/cl.190403
• 参照: Thermal Metathesis of C–C Single Bonds Induced by Steric Frustration; https://cir.nii.ac.jp/crid/1360016862083892992
• 参照: Reductive Cross‐Coupling Reactions between Two Electrophiles; https://cir.nii.ac.jp/crid/1360011143797623808; Mechanism and Selectivity in Nickel-Catalyzed Cross-Electrophile Coupling of Aryl Halides with Alkyl Halides; https://cir.nii.ac.jp/crid/1360011145355999744; Salt‐Free Reduction of Nonprecious Transition‐Metal Compounds: Generation of Amorphous Ni Nanoparticles for Catalytic C–C Bond Formation; https://cir.nii.ac.jp/crid/1360283689401851648; Aryl Ketones as Single‐Electron‐Transfer Photoredox Catalysts in the Nickel‐Catalyzed Homocoupling of Aryl Halides; https://cir.nii.ac.jp/crid/1360285705079462144; Preparation of Ni(cod)₂ Using Light as the Source of Energy; https://cir.nii.ac.jp/crid/1360285708118143232; Complexation with diol host compounds. Part 2. Structures of 1,1,2,2-tetraphenylethane-1,2-diol and its 1?2 molecular inclusion complex with dimethylsulphoxide; https://cir.nii.ac.jp/crid/1360574095052828928; Nickel-Catalyzed Reductive Cross-Coupling of Aryl Halides with Alkyl Halides; https://cir.nii.ac.jp/crid/1360574096095388032; Reactivity of ketyl free radicals. Part 2.—Dimerization and dismutation of fluorenone and xanthone ketyls; https://cir.nii.ac.jp/crid/1360574096293743488; Bimetallic C–C Bond-Forming Reductive Elimination from Nickel; https://cir.nii.ac.jp/crid/1360855571123050112; 1,2-Ethanediol (Ethylene Glycol) at 130K; https://cir.nii.ac.jp/crid/1360855571149509248; Crystalline ethane-1,2-diol does not have intra-molecular hydrogen bonding: Experimental and theoretical charge density studies; https://cir.nii.ac.jp/crid/1361137043533928064; Reaction of .pi.-allylnickel bromide complexes with organic halides. Stereochemistry and mechanism; https://cir.nii.ac.jp/crid/1361137043906532736; Electronic Interaction in Ketyl Radicals; https://cir.nii.ac.jp/crid/1361418518558515968; Nickel‐Catalyzed Cross‐Electrophile Coupling with Organic Reductants in Non‐Amide Solvents; https://cir.nii.ac.jp/crid/1361418519468000768; Synthesis with zerovalent nickel. Coupling of aryl halides with bis(1,5-cyclooctadiene)nickel(0); https://cir.nii.ac.jp/crid/1361418519666484608; Coupling of aryl chlorides by nickel and reducing metals; https://cir.nii.ac.jp/crid/1361418520087156992; generation of a solvated zerovalent nickel reagent. Biaryl formation; https://cir.nii.ac.jp/crid/1361699993859586944; 2,3-Dimethyl-2,3-butanediol (pinacol); https://cir.nii.ac.jp/crid/1361699993878648832; Nickel-phosphine complex-catalyzed homo coupling of aryl halides in the presence of zinc powder; https://cir.nii.ac.jp/crid/1361699995646415616; Structures and vibrational spectra of pinacol. Part 2. A new crystal form of pinacol: a key to the infrared spectroscopic identification of the G and T conformers in condensed phases; https://cir.nii.ac.jp/crid/1361699996182850432; Palladium-Catalyzed Tetrakis(dimethylamino)ethylene-Promoted Reductive Coupling of Aryl Halides; https://cir.nii.ac.jp/crid/1361981469583277184; Nickel-catalyzed reductive coupling of alkyl halides with other electrophiles: concept and mechanistic considerations; https://cir.nii.ac.jp/crid/1361981470097548800; Methods and Mechanisms for Cross-Electrophile Coupling of Csp² Halides with Alkyl Electrophiles; https://cir.nii.ac.jp/crid/1362262945445052800; Mechanism of CC coupling reactions of aromatic halides, promoted by Ni(COD)2 in the presence of 2,2′-bipyridine and PPh3, to give biaryls; https://cir.nii.ac.jp/crid/1362544420913705600; Mechanism of biaryl synthesis with nickel complexes; https://cir.nii.ac.jp/crid/1362544421120002304; BENZOPINACOL; https://cir.nii.ac.jp/crid/1363388844950190720; Aryl−Aryl Bond Formation One Century after the Discovery of the Ullmann Reaction; https://cir.nii.ac.jp/crid/1363388845863546240; First Isolation of a Metal Ketyl in Aggregated Forms. X-ray Structures of Dimeric and Tetrameric Sodium Fluorenone Ketyl Complexes: [Na(μ₂-η¹-ketyl)(HMPA)₂]₂ and [Na(μ₃-η¹-ketyl)(HMPA)]₄; https://cir.nii.ac.jp/crid/1363670319443539712; Lithium Hydride Mediated Nickel(0) Catalysed Biaryl Synthesis from Aryl Chlorides and Bromides; https://cir.nii.ac.jp/crid/1363951794194043520; .sigma.-Aryl compounds of nickel, palladium, and platinum. Synthesis and bonding studies; https://cir.nii.ac.jp/crid/1364233269110869760; Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Alkyl Bromides: Et₃N as the Terminal Reductant; https://cir.nii.ac.jp/crid/1364233271232557568
• 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: 雑誌記事索引データベース; https://ndlsearch.ndl.go.jp; Crossref; https://www.crossref.org; CiNii Articles; 科学研究費助成事業データベース; https://kaken.nii.ac.jp/ja
• 書誌ID（NDLBibID）: 11552465; http://id.ndl.go.jp/bib/11552465
• NII論文ID: 130007703046