One-pot sequential fluorostannylation-arylstannylation of arynes

• Material Type: 記事
• Title: One-pot sequential fluorostannylation-arylstannylation of arynes
• Author/Editor: Hideya Tanaka; Itaru Osaka; Hiroto Yoshida
• Publication, Distribution, etc.: 日本 : The Chemical Society of Japan
• Publication Date: 2019-06-05
• Publication Date (W3CDTF): 2019-06-05
• Periodical title: Chemistry letters
• No. or year of volume/issue: 48(9)
• Volume: 48(9)
• ISSN (Periodical Title): 1348-0715
• ISSN-L (Periodical Title): 0366-7022
• Text Language Code: eng
• DOI: 10.1246/cl.190385; https://doi.org/10.1246/cl.190385
• Persistent ID (NDL): info:ndljp/pid/11552463; https://dl.ndl.go.jp/pid/11552463
• Collection: 障害者向け資料
• Collection (Materials For Handicapped People:1): テキストデータ
• Collection (particular): 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
• Acquisition Basis: オンライン資料収集制度
• Date Accepted (W3CDTF): 2020-10-07T08:55:27+09:00
• Date Captured (W3CDTF): 2019-08-21
• Format (IMT): application/pdf
• Access Restrictions: 国立国会図書館内限定公開
• Service for the Digitized Contents Transmission Service: 図書館・個人送信対象外
• Availability of remote photoduplication service: 可
• Periodical Title (URI): https://www.journal.csj.jp/toc/cl/48/9
• Periodical Title (Persistent ID (NDL)): info:ndljp/pid/11552460; https://dl.ndl.go.jp/pid/11552460
• Data Provider (Database): 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

• Summary, etc.: 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.190385; https://doi.org/10.1246/cl.190385
• Related Material (URI): http://id.ndl.go.jp/digimeta/11552463; https://dl.ndl.go.jp/pid/11552463; http://www.journal.csj.jp/doi/pdf/10.1246/cl.190385
• Is Referenced By: Synthesis of Diverse γ-Aryl-β-ketoesters via Aryne Intermediates Generated by C–C Bond Cleavage; https://cir.nii.ac.jp/crid/1360005518010669184; Synthesis of Multisubstituted Benzenes from Phenols via Multisubstituted Benzynes; https://cir.nii.ac.jp/crid/1360298757448730240; Acylalkylation of Arynes Generated from <i>o</i>-Iodoaryl Triflates with Hydrosilanes and Cesium Fluoride; https://cir.nii.ac.jp/crid/1360572092624897536; Synthesis of Functionalized Benzopyran/Coumarin-Derived Aryne Precursors and Their Applications; https://cir.nii.ac.jp/crid/1360853567601600128; Reaction mechanism with indano[60]fullerene bromide for evaporable fullerene derivatives; https://cir.nii.ac.jp/crid/1360869855110152960; フッ素化反応2010-2020; https://cir.nii.ac.jp/crid/1390008166736795008; Synthesis of phenoxathiins and phenothiazines by aryne reactions with thiosulfonates; https://cir.nii.ac.jp/crid/2050588892102342144
• References: Copper-Catalyzed Borylstannylation of Alkynes with Tin Fluorides; https://cir.nii.ac.jp/crid/1050303564712861824; Ligand‐Free Copper‐Catalyzed Cyano‐ and Alkynylstannylation of Arynes; https://cir.nii.ac.jp/crid/1050303564713650176; Copper Catalysis for Synthesizing Main-Group Organometallics Containing B, Sn or Si; https://cir.nii.ac.jp/crid/1050585039688926336; Copper-catalyzed α-selective hydrostannylation of alkynes for the synthesis of branched alkenylstannanes; https://cir.nii.ac.jp/crid/1050585039690393984; Inverse regioselectivity in the silylstannylation of alkynes and allenes: copper-catalyzed three-component coupling with a silylborane and a tin alkoxide; https://cir.nii.ac.jp/crid/1050866514667105792; Silver-Catalyzed Late-Stage Fluorination; https://cir.nii.ac.jp/crid/1360292619261816832; FLUORIDE-INDUCED 1,2-ELIMINATION OF <i>O</i>-TRIMETHYLSILYLPHENYL TRIFLATE TO BENZYNE UNDER MILD CONDITIONS; https://cir.nii.ac.jp/crid/1360565169060698624; Silver-Mediated Fluorination of Functionalized Aryl Stannanes; https://cir.nii.ac.jp/crid/1360574094367311488; Copper-catalyzed arylstannylation of arynes in a sequence; https://cir.nii.ac.jp/crid/1360849943436373504; Tin in Organic Synthesis; https://cir.nii.ac.jp/crid/1360855570320530688; Borylstannylation of alkynes with inverse regioselectivity: copper-catalyzed three-component coupling using a masked diboron; https://cir.nii.ac.jp/crid/1361137044077982848; Copper-catalyzed distannylation of alkynes; https://cir.nii.ac.jp/crid/1361418519149997824; The Stille Reaction, 38 Years Later; https://cir.nii.ac.jp/crid/1361981469187908224; Metal-Catalyzed Hydrostannations; https://cir.nii.ac.jp/crid/1361981469388573056; Copper‐Catalyzed Three‐Component Borylstannylation of Alkynes; https://cir.nii.ac.jp/crid/1361981470054392320; Stannylation Reactions under Base Metal Catalysis: Some Recent Advances; https://cir.nii.ac.jp/crid/1362544418728046976; Facile Access to vic-Borylstannylalkanes via Copper-Catalyzed Three-Component Borylstannylation of Alkenes; https://cir.nii.ac.jp/crid/1362544420239781376; Synchronous ArF and ArSn Bond Formation through Fluorostannylation of Arynes; https://cir.nii.ac.jp/crid/1362544420869905280; Synthesis of biaryls using aryne intermediates; https://cir.nii.ac.jp/crid/1362825893276938496; Radiosynthesis and Evaluation of [¹⁸F]Selectfluor bis(triflate); https://cir.nii.ac.jp/crid/1363670320294060672; Organotin Reagents in Cross‐Coupling Reactions; https://cir.nii.ac.jp/crid/1364233268747836544; Allylstannanes and vinylstannanes from stannylcupration of C–C multiple bonds. Recent advances and applications in organic synthesis; https://cir.nii.ac.jp/crid/1364233269975580416
• Data Provider (Database): 国立情報学研究所 : CiNii Research; https://cir.nii.ac.jp/
• Original Data Provider (Database): 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
• Bibliographic ID (NDL): 11552463; http://id.ndl.go.jp/bib/11552463
• NAID: 130007703025