Pyridazine synthesis from 1,2,4,5-tetrazines and alkynes in 1,1,1,3,3,3-hexafluoro-2-propanol through the inverse electron demand Diels-Alder reaction

• 資料種別: 記事
• タイトル: Pyridazine synthesis from 1,2,4,5-tetrazines and alkynes in 1,1,1,3,3,3-hexafluoro-2-propanol through the inverse electron demand Diels-Alder reaction
• 著者・編者: Chika Yamamoto; Minori Suzuki; Suguru Yoshida
• 出版事項: 日本 : The Chemical Society of Japan
• 出版年月日等: 2022-11-18
• 出版年（W3CDTF）: 2022-11-18
• タイトル（掲載誌）: Bulletin of the Chemical Society of Japan
• 巻号年月日等（掲載誌）: 95(12)
• 掲載巻: 95(12)
• 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.20220267; https://doi.org/10.1246/bcsj.20220267
• 国立国会図書館永続的識別子: info:ndljp/pid/12686466; https://dl.ndl.go.jp/pid/12686466
• 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/95/12
• 掲載誌（国立国会図書館永続的識別子）: info:ndljp/pid/12686465; https://dl.ndl.go.jp/pid/12686465
• 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.20220267; https://doi.org/10.1246/bcsj.20220267
• 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/12686466; https://dl.ndl.go.jp/pid/12686466; https://academic.oup.com/bcsj/article-pdf/95/12/1741/56315269/bcsj.20220267.pdf
• 参照: Recent Advancements in Novel Sensing Systems through Nanoarchitectonics; https://cir.nii.ac.jp/crid/1360021390564221952; Synthesis of Fluorenones and Xanthones through Intramolecular C–F Arylation; https://cir.nii.ac.jp/crid/1360579814363626752; Regioselective pyridazine synthesis from tetrazines and alkynyl sulfides; https://cir.nii.ac.jp/crid/1360588381077125120; Three-step click assembly using trivalent platforms bearing azido, ethynyl, and fluorosulfonyl groups; https://cir.nii.ac.jp/crid/1360869854357988736
• 参照: 3,6-Substituted-1,2,4,5-tetrazines: tuning reaction rates for staged labeling applications; https://cir.nii.ac.jp/crid/1360011146331358208; A genetically encoded cyclobutene probe for labelling of live cells; https://cir.nii.ac.jp/crid/1360016865835186304; Biodegradable Tetra-PEG Hydrogels as Carriers for a Releasable Drug Delivery System; https://cir.nii.ac.jp/crid/1360016866983756544; Divergent Synthesis of Monosubstituted and Unsymmetrical 3,6‐Disubstituted Tetrazines from Carboxylic Ester Precursors; https://cir.nii.ac.jp/crid/1360016867529005568; Reaktionen sechsgliedriger heterocyclen mit ketenacetalen; https://cir.nii.ac.jp/crid/1360016870423307008; Synergistic Experimental and Computational Investigation of the Bioorthogonal Reactivity of Substituted Aryltetrazines; https://cir.nii.ac.jp/crid/1360016870447756800; Site-Specific Antibody Functionalization Using Tetrazine–Styrene Cycloaddition; https://cir.nii.ac.jp/crid/1360016870613935872; Tetrazine Ligation: Fast Bioconjugation Based on Inverse-Electron-Demand Diels−Alder Reactivity; https://cir.nii.ac.jp/crid/1360292620276593920; Design and Synthesis of Aza‐Bicyclononene Dienophiles for Rapid Fluorogenic Ligations; https://cir.nii.ac.jp/crid/1360298341336870400; Pyridazine as a privileged structure: An updated review on anticancer activity of pyridazine containing bioactive molecules; https://cir.nii.ac.jp/crid/1360298342495237248; Mechanism‐Based Fluorogenic <i>trans</i>‐Cyclooctene–Tetrazine Cycloaddition; https://cir.nii.ac.jp/crid/1360298343891201280; Metal‐Free Synthetic Approach to 3‐Monosubstituted Unsymmetrical 1,2,4,5‐Tetrazines Useful for Bioorthogonal Reactions; https://cir.nii.ac.jp/crid/1360298345308821248; Highly Stable and Selective Tetrazines for the Coordination-Assisted Bioorthogonal Ligation with Vinylboronic Acids; https://cir.nii.ac.jp/crid/1360298345575632896; Tetrazine ligation for chemical proteomics; https://cir.nii.ac.jp/crid/1360579817345437184; To View Your Biomolecule, Click inside the Cell; https://cir.nii.ac.jp/crid/1360579819725927552; Mutually Orthogonal Bioconjugation of Vinyl Nucleosides for RNA Metabolic Labeling; https://cir.nii.ac.jp/crid/1360579820404987392; Synthesis of 3,5-disubstituted pyridazines by regioselective [4+2] cycloadditions with ethynyltributyltin and subsequent replacement of the organotin substituent; https://cir.nii.ac.jp/crid/1360861291110376448; Fluorogenic protein labeling using a genetically encoded unstrained alkene; https://cir.nii.ac.jp/crid/1360861291209332480; HFIP in Organic Synthesis; https://cir.nii.ac.jp/crid/1360861294960161024; Synthesis of 3-monosubstituted s-tetrazines and their reactions with monosubstituted acetylenes; https://cir.nii.ac.jp/crid/1360861295198554496; Uncovering the Key Role of Distortion in Bioorthogonal Tetrazine Tools That Defy the Reactivity/Stability Trade-Off; https://cir.nii.ac.jp/crid/1360861295472798848; Origin of Increased Reactivity in Rhenium-Mediated Cycloadditions of Tetrazines; https://cir.nii.ac.jp/crid/1360861295478342912; Inverse electron demand Diels–Alder (iEDDA)-initiated conjugation: a (high) potential click chemistry scheme; https://cir.nii.ac.jp/crid/1361137045961268992; Fluorinated Alcohols: A New Medium for Selective and Clean Reaction; https://cir.nii.ac.jp/crid/1361418519022822656; Vinylboronic Acids as Fast Reacting, Synthetically Accessible, and Stable Bioorthogonal Reactants in the Carboni–Lindsey Reaction; https://cir.nii.ac.jp/crid/1361418521222358784; Clicking 1,2,4,5-tetrazine and cyclooctynes with tunable reaction rates; https://cir.nii.ac.jp/crid/1361699993515204224; Fluorine-Directed Nazarov Cyclizations: A Controlled Synthesis of Cross-Conjugated 2-Cyclopenten-1-ones; https://cir.nii.ac.jp/crid/1361699993712326656; Silyl‐Derivate von Pyridazin; https://cir.nii.ac.jp/crid/1361699995257436672; Fast and Sensitive Pretargeted Labeling of Cancer Cells through a Tetrazine/ <i>trans</i> ‐Cyclooctene Cycloaddition; https://cir.nii.ac.jp/crid/1361981469071977216; Fluoroalcohols: versatile solvents in hypervalent iodine chemistry and syntheses of diaryliodonium(III) salts; https://cir.nii.ac.jp/crid/1361981469547962624; Inverse electron demand Diels–Alder reactions in chemical biology; https://cir.nii.ac.jp/crid/1362262945596310016; Protein Degradation by In-Cell Self-Assembly of Proteolysis Targeting Chimeras; https://cir.nii.ac.jp/crid/1362544419016614400; Reaktivität einfacher offenkettiger und cyclischer dienophile bei Diels-Alder-reaktionen mit inversem elektronenbedarf; https://cir.nii.ac.jp/crid/1362544421270626560; Acylazetine as a Dienophile in Bioorthogonal Inverse Electron-Demand Diels–Alder Ligation; https://cir.nii.ac.jp/crid/1363107370121479040; A trifunctional linker suitable for conducting three orthogonal click chemistries in one pot; https://cir.nii.ac.jp/crid/1363388845901905792
• 参照（URI）: https://cir.nii.ac.jp/crid/1370579811505908864
• 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; 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）: 12686466; http://id.ndl.go.jp/bib/12686466