Effect of resonance on the clickability of alkenyl azides in the strain-promoted cycloaddition with dibenzo-fused cyclooctynes
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- 資料種別
- 記事
- 著者・編者
- Suguru YoshidaSayuri GotoYoshitake Nishiyama
- 出版年月日等
- 2019-06-05
- 出版年（W3CDTF）
- 2019-06-05
- 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.190400
- 国立国会図書館永続的識別子
- info:ndljp/pid/11552464
- コレクション（共通）
- コレクション（障害者向け資料：レベル1）
- 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
- 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（国立国会図書館永続的識別子）
- info:ndljp/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
- 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.190400
- 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）
- 参照
- 2-Azidoacrylamides as compact platforms for efficient modular synthesisTaming the reactivity of alkyl azides by intramolecular hydrogen bonding: site-selective conjugation of unhindered diazidesNucleophilic transformations of azido-containing carbonyl compounds <i>via</i> protection of the azido groupSelective strain-promoted azide–alkyne cycloadditions through transient protection of bicyclo[6.1.0]nonynes with silver or goldAssembly of four modules onto a tetraazide platform by consecutive 1,2,3-triazole formations(Hexafluoroacetylacetonato)copper(<scp>i</scp>)–cycloalkyne complexes as protected cycloalkynesSpot the difference in reactivity: a comprehensive review of site-selective multicomponent conjugation exploiting multi-azide compounds
- 参照
- Formal C–H‐Azidation – Based Shortcut to Diazido Building Blocks for the Versatile Preparation of Photoaffinity Labeling ProbesTransient Protection of Organic Azides from Click Reactions with Alkynes by Phosphazide FormationTransient Protection of Strained Alkynes from Click Reaction via Complexation with CopperSite-selective conversion of azido groups at carbonyl α-positions into oxime groups leading triazide to a triple click conjugation scaffoldThieme Chemistry Journals Awardees: Where Are They Now? One-Pot Synthesis of Versatile Buckle Units for Click Chemistry: 4,8-Diazacyclononynes (DACNs)2-Aminobenzenesulfonamide-Containing Cyclononyne as Adjustable Click Reagent for Strain-Promoted Azide–Alkyne CycloadditionClick Chemistry in Materials ScienceClick Chemistry in Complex Mixtures: Bioorthogonal BioconjugationTransition States of Strain-Promoted Metal-Free Click Chemistry: 1,3-Dipolar Cycloadditions of Phenyl Azide and CyclooctynesConvergent synthesis of trifunctional molecules by three sequential azido-type-selective cycloadditionsCu-Catalyzed Azide−Alkyne CycloadditionZur Existenz niedergliedriger Cycloalkine, IAza-dibenzocyclooctynes for fast and efficient enzyme PEGylation via copper-free (3+2) cycloadditionFurther enhancement of the clickability of doubly sterically-hindered aryl azides by <i>para</i>-amino substitutionStrain-Promoted 1,3-Dipolar Cycloaddition of Cycloalkynes and Organic AzidesNovel bifunctional probe for radioisotope-free photoaffinity labeling: compact structure comprised of photospecific ligand ligation and detectable tag anchoring unitsElectronic supplementary information (ESI) available: Photo-decomposition study of phenyl and benzyl azides. Experimental details for photoreactions of 1 and 5. Synthetic procedures and characterization of new compounds. See http://www.rsc.org/suppdata/ob/b3/b316221d/.Chemoselective Layer-by-Layer Approach Utilizing Click Reactions with Ethynylcyclooctynes and DiazidesSubstituted 5,6,11,12-Tetradehydrodibenzo[<i>a</i>,<i>e</i>]cyclooctenes: Syntheses, Properties, and DFT Studies of Substituted Sondheimer–Wong DiynesStaudinger reaction using 2,6-dichlorophenyl azide derivatives for robust aza-ylide formation applicable to bioconjugation in living cellsA facile preparation of functional cycloalkynes <i>via</i> an azide-to-cycloalkyne switching approachRecent Advances in Reactions of AzidesIn Vivo Imaging of Membrane-Associated Glycans in Developing ZebrafishEnhanced clickability of doubly sterically-hindered aryl azidesA Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living SystemsFacile synthesis of diazido-functionalized biaryl compounds as radioisotope-free photoaffinity probes by Suzuki–Miyaura couplingHighly accelerated inverse electron-demand cycloaddition of electron-deficient azides with aliphatic cyclooctynesHeteroatom‐embedded Medium‐Sized Cycloalkynes: Concise Synthesis, Structural Analysis, and ReactionsReadily Accessible Bicyclononynes for Bioorthogonal Labeling and Three‐Dimensional Imaging of Living CellsOrthogonal synthesis of pyrroles and 1,2,3-triazoles from vinyl azides and 1,3-dicarbonyl compoundsBioorthogonal Chemistry: Fishing for Selectivity in a Sea of FunctionalityChemoselectivity of Tertiary Azides in Strain‐Promoted Alkyne‐Azide CycloadditionsDesign of dantrolene-derived probes for radioisotope-free photoaffinity labeling of proteins involved in the physiological Ca2+ release from sarcoplasmic reticulum of skeletal muscleSite-Selective Conversion of Azido Groups at Carbonyl α-Positions to Diazo Groups in Diazido and Triazido CompoundsUnsaturated eight-membered ring compounds. XI. Synthesis of sym-dibenzo-1,5-cyclooctadiene-3,7-diyne and sym-dibenzo-1,3,5-cyclooctatrien-7-yne, presumably planar conjugated eight-membered ring compoundsThe Chemistry of Unusually Functionalized AzidesClick Chemistry for Drug Development and Diverse Chemical–Biology ApplicationsCu-free click cycloaddition reactions in chemical biologySecond-Generation Difluorinated Cyclooctynes for Copper-Free Click ChemistryAzide: A Unique Dipole for Metal‐Free Bioorthogonal LigationsCopper‐Free Click Reactions with Polar Bicyclononyne Derivatives for Modulation of Cellular ImagingStrain-promoted double-click reaction for chemical modification of azido-biomolecules1,3-Dipolar Cycloaddition Reactivities of Perfluorinated Aryl Azides with Enamines and Strained DipolarophilesVisualizing Metabolically Labeled Glycoconjugates of Living Cells by Copper‐Free and Fast Huisgen CycloadditionsOrganic Azides: An Exploding Diversity of a Unique Class of CompoundsRapid Cu-Free Click Chemistry with Readily Synthesized BiarylazacyclooctynonesSelective Labeling of Living Cells by a Photo-Triggered Click ReactionRecent Advances in Recoverable Systems for the Copper-Catalyzed Azide-Alkyne Cycloaddition Reaction (CuAAC)Copper-catalyzed azide–alkyne cycloaddition (CuAAC) and beyond: new reactivity of copper(i) acetylidesFine-Tuning Strain and Electronic Activation of Strain-Promoted 1,3-Dipolar Cycloadditions with Endocyclic Sulfamates in SNO-OCTsDistortion/Interaction Energy Control of 1,3-Dipolar Cycloaddition ReactivityClick Chemistry for Biotechnology and Materials ScienceSynthesis of TRIPCO: A New Cyclooctyne for iSPAACChemoselective Sequential “Click” Ligation Using Unsymmetrical BisazidesOrganic AzidesPeptidotriazoles on Solid Phase: [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides90th Commemorative Account : Fascinating Molecules and Reactions : Award Account : Controlled Reactive Intermediates Enabling Facile Molecular ConjugationSequential molecular conjugation using thiophene S,S-dioxides bearing a clickable functional group
- 参照（URI）
- 連携機関・データベース
- 国立情報学研究所 : CiNii Research
- 提供元機関・データベース
- 雑誌記事索引データベースCrossrefCiNii Articles科学研究費助成事業データベース科学研究費助成事業データベース科学研究費助成事業データベース科学研究費助成事業データベースCrossrefCrossrefCrossrefCrossrefCrossrefCrossrefCrossref
- 書誌ID（NDLBibID）
- 11552464
- NII論文ID
- 130007703048