{"@context":{"@vocab":"https://cir.nii.ac.jp/schema/1.0/","rdfs":"http://www.w3.org/2000/01/rdf-schema#","dc":"http://purl.org/dc/elements/1.1/","dcterms":"http://purl.org/dc/terms/","foaf":"http://xmlns.com/foaf/0.1/","prism":"http://prismstandard.org/namespaces/basic/2.0/","cinii":"http://ci.nii.ac.jp/ns/1.0/","datacite":"https://schema.datacite.org/meta/kernel-4/","ndl":"http://ndl.go.jp/dcndl/terms/","jpcoar":"https://github.com/JPCOAR/schema/blob/master/2.0/"},"@id":"https://cir.nii.ac.jp/crid/1360004233142659072.json","@type":"Article","productIdentifier":[{"identifier":{"@type":"DOI","@value":"10.1021/acs.orglett.8b01692"}},{"identifier":{"@type":"URI","@value":"https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b01692"}},{"identifier":{"@type":"PMID","@value":"29901399"}}],"resourceType":"学術雑誌論文(journal article)","dc:title":[{"@value":"Transient Protection of Organic Azides from Click Reactions with Alkynes by Phosphazide Formation"}],"description":[{"notation":[{"@value":"A method for protecting organic azides from click reactions with alkynes is reported. Treatment of azides with Amphos affords phosphazides, which are stable under click reaction conditions and are easily converted back to azides by treatment with elemental sulfur. Thus, the method allows for facile modification of azide compounds via site-selective click reactions."}]}],"creator":[{"@id":"https://cir.nii.ac.jp/crid/1380004233142659074","@type":"Researcher","foaf:name":[{"@value":"Tomohiro Meguro"}],"jpcoar:affiliationName":[{"@value":"Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU), 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004233142659075","@type":"Researcher","foaf:name":[{"@value":"Suguru Yoshida"}],"jpcoar:affiliationName":[{"@value":"Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU), 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004233142659076","@type":"Researcher","foaf:name":[{"@value":"Kazunobu Igawa"}],"jpcoar:affiliationName":[{"@value":"Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-koen, Kasuga, Fukuoka 816-8580, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1380004233142659073","@type":"Researcher","foaf:name":[{"@value":"Katsuhiko Tomooka"}],"jpcoar:affiliationName":[{"@value":"Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-koen, Kasuga, Fukuoka 816-8580, Japan"}]},{"@id":"https://cir.nii.ac.jp/crid/1420001326222513408","@type":"Researcher","personIdentifier":[{"@type":"KAKEN_RESEARCHERS","@value":"60273124"},{"@type":"NRID","@value":"1000060273124"},{"@type":"ORCID","@value":"0000-0002-7270-351X"},{"@type":"NRID","@value":"9000411077402"},{"@type":"NRID","@value":"9000403168475"},{"@type":"NRID","@value":"9000016987875"},{"@type":"NRID","@value":"9000001997016"},{"@type":"NRID","@value":"9000345257111"},{"@type":"NRID","@value":"9000353371877"},{"@type":"NRID","@value":"9000326666116"},{"@type":"NRID","@value":"9000345337665"},{"@type":"NRID","@value":"9000307260952"},{"@type":"NRID","@value":"9000409599805"},{"@type":"NRID","@value":"9000408919892"},{"@type":"NRID","@value":"9000365518442"},{"@type":"NRID","@value":"9000379072977"},{"@type":"NRID","@value":"9000290131655"},{"@type":"NRID","@value":"9000404110007"},{"@type":"NRID","@value":"9000404315267"},{"@type":"NRID","@value":"9000404315397"},{"@type":"NRID","@value":"9000019188936"},{"@type":"NRID","@value":"9000006704037"},{"@type":"NRID","@value":"9000362235845"},{"@type":"NRID","@value":"9000402818991"},{"@type":"NRID","@value":"9000404845284"},{"@type":"NRID","@value":"9000403437089"},{"@type":"NRID","@value":"9000257737878"},{"@type":"NRID","@value":"9000368417648"},{"@type":"NRID","@value":"9000326648740"},{"@type":"NRID","@value":"9000413750908"},{"@type":"NRID","@value":"9000406399329"},{"@type":"NRID","@value":"9000291894956"},{"@type":"NRID","@value":"9000365620328"},{"@type":"NRID","@value":"9000347546119"},{"@type":"NRID","@value":"9000406309563"},{"@type":"NRID","@value":"9000301747889"},{"@type":"NRID","@value":"9000415350044"},{"@type":"NRID","@value":"9000403437556"},{"@type":"NRID","@value":"9000002040531"},{"@type":"NRID","@value":"9000369354253"},{"@type":"NRID","@value":"9000311788619"},{"@type":"NRID","@value":"9000391957772"},{"@type":"NRID","@value":"9000415233075"},{"@type":"NRID","@value":"9000345337580"},{"@type":"NRID","@value":"9000413380905"},{"@type":"NRID","@value":"9000398129991"},{"@type":"NRID","@value":"9000261046632"},{"@type":"NRID","@value":"9000350668841"},{"@type":"NRID","@value":"9000410155252"},{"@type":"NRID","@value":"9000398303566"},{"@type":"NRID","@value":"9000397821223"},{"@type":"NRID","@value":"9000399766503"},{"@type":"NRID","@value":"9000258600476"},{"@type":"NRID","@value":"9000309998909"},{"@type":"NRID","@value":"9000411114914"},{"@type":"NRID","@value":"9000409599786"},{"@type":"NRID","@value":"9000409599889"},{"@type":"NRID","@value":"9000398403314"},{"@type":"NRID","@value":"9000017181181"},{"@type":"NRID","@value":"9000020077942"},{"@type":"NRID","@value":"9000396144416"},{"@type":"NRID","@value":"9000258600538"},{"@type":"NRID","@value":"9000391963041"},{"@type":"NRID","@value":"9000399767030"},{"@type":"NRID","@value":"9000000009698"},{"@type":"NRID","@value":"9000329440268"},{"@type":"NRID","@value":"9000345337649"},{"@type":"NRID","@value":"9000404628927"},{"@type":"RESEARCHMAP","@value":"https://researchmap.jp/read0125580"}],"foaf:name":[{"@value":"Takamitsu Hosoya"}],"jpcoar:affiliationName":[{"@value":"Laboratory of Chemical Bioscience, Institute of Biomaterials and Bioengineering, Tokyo Medical and Dental University (TMDU), 2-3-10 Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan"}]}],"publication":{"publicationIdentifier":[{"@type":"PISSN","@value":"15237060"},{"@type":"EISSN","@value":"15237052"}],"prism:publicationName":[{"@value":"Organic Letters"}],"dc:publisher":[{"@value":"American Chemical Society (ACS)"}],"prism:publicationDate":"2018-06-14","prism:volume":"20","prism:number":"13","prism:startingPage":"4126","prism:endingPage":"4130"},"reviewed":"false","url":[{"@id":"https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b01692"}],"createdAt":"2018-06-14","modifiedAt":"2023-04-27","project":[{"@id":"https://cir.nii.ac.jp/crid/1040000781994444672","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"18H04386"},{"@type":"JGN","@value":"JP18H04386"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PUBLICLY-18H04386/"}],"notation":[{"@language":"ja","@value":"異種アジド基の選択的な利用を鍵とする機能性中分子の迅速合成法の開発"}]},{"@id":"https://cir.nii.ac.jp/crid/1040282256936406784","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"17H06414"},{"@type":"JGN","@value":"JP17H06414"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PLANNED-17H06414/"}],"notation":[{"@language":"ja","@value":"ミトコンドリア、ゴルジ体に関連する応答ゾーン、連携ゾーン解析"},{"@language":"en","@value":"Analysis of \"Response zone\" and \" Communication zone\" in mitochondria and Golgi apparatus"}]},{"@id":"https://cir.nii.ac.jp/crid/1040282256969740032","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"18H02104"},{"@type":"JGN","@value":"JP18H02104"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18H02104/"}],"notation":[{"@language":"ja","@value":"実践的プローブ分子開発のためのクリックケミストリーの新展開"},{"@language":"en","@value":"Innovative click chemistry for development of practical molecular probes"}]},{"@id":"https://cir.nii.ac.jp/crid/1040282256972370944","@type":"Project","projectIdentifier":[{"@type":"KAKEN","@value":"18J11113"},{"@type":"JGN","@value":"JP18J11113"},{"@type":"URI","@value":"https://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-18J11113/"}],"notation":[{"@language":"ja","@value":"アジド基の保護法を基軸にした多機能性分子の簡便構築法の開発"}]}],"relatedProduct":[{"@id":"https://cir.nii.ac.jp/crid/1360004230102011904","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Formal C–H‐Azidation – Based Shortcut to Diazido Building Blocks for the Versatile Preparation of Photoaffinity Labeling Probes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233213917184","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Transient Protection of Strained Alkynes from Click Reaction via Complexation with Copper"}]},{"@id":"https://cir.nii.ac.jp/crid/1360004233625378176","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Site-selective conversion of azido groups at carbonyl α-positions into oxime groups leading triazide to a triple click conjugation scaffold"}]},{"@id":"https://cir.nii.ac.jp/crid/1360009142671787136","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Triazole formation of phosphinyl alkynes with azides through transient protection of phosphine by copper"}]},{"@id":"https://cir.nii.ac.jp/crid/1360009142671798528","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"2-Azidoacrylamides as compact platforms for efficient modular synthesis"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011143608169984","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"2-Aminobenzenesulfonamide-Containing Cyclononyne as Adjustable Click Reagent for Strain-Promoted Azide–Alkyne Cycloaddition"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144034182016","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Constrained‐Geometry Bisphosphazides Derived from 1,8‐Diazidonaphthalene: Synthesis, Spectroscopic Characteristics, Structural Features, and Theoretical Investigations"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144336560640","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Phosphine‐Mediated Conversion of Azides into Diazo Compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144367108864","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Click Chemistry in Materials Science"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011144837147520","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Orthogonal bioorthogonal chemistries"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011145813448704","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chemoselective preparation of disymmetric bistriazoles from bisalkynes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360011146570145664","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ultrafast Click Chemistry with Fluorosydnones"}]},{"@id":"https://cir.nii.ac.jp/crid/1360013168762776448","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Taming the reactivity of alkyl azides by intramolecular hydrogen bonding: site-selective conjugation of unhindered diazides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360013168800972928","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Nucleophilic transformations of azido-containing carbonyl compounds <i>via</i> protection of the azido group"}]},{"@id":"https://cir.nii.ac.jp/crid/1360017282188809088","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Substitution of α-Azido Sulfones with Thiolates to Form α-Azido Sulfides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285708601192576","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Convergent synthesis of trifunctional molecules by three sequential azido-type-selective cycloadditions"}]},{"@id":"https://cir.nii.ac.jp/crid/1360285714738029568","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Diverse 3-Azido-5-(azidomethyl)benzene Derivatives via Formal C–H Azidation and Functional Group-Selective Transformations"}]},{"@id":"https://cir.nii.ac.jp/crid/1360290617648472192","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Selective strain-promoted azide–alkyne cycloadditions through transient protection of bicyclo[6.1.0]nonynes with silver or gold"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292618627912704","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cu-Catalyzed Azide−Alkyne Cycloaddition"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620114785152","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chemoselective Sequential Click Ligations Directed by Enhanced Reactivity of an Aromatic Ynamine"}]},{"@id":"https://cir.nii.ac.jp/crid/1360292620594768512","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chain‐Growth Click Polymerization of AB<sub>2</sub> Monomers for the Formation of Hyperbranched Polymers with Low Polydispersities in a One‐Pot Process"}]},{"@id":"https://cir.nii.ac.jp/crid/1360302864790534144","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Amphos-Mediated Conversion of Alkyl Azides to Diazo Compounds and One-Pot Azide-Site Selective Transient Protection, Click Conjugation, and Deprotective Transformation"}]},{"@id":"https://cir.nii.ac.jp/crid/1360302864804864128","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of 1,2,3-triazoles using Grignard reactions through the protection of azides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360567183578404864","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Further enhancement of the clickability of doubly sterically-hindered aryl azides by <i>para</i>-amino substitution"}]},{"@id":"https://cir.nii.ac.jp/crid/1360572092625234048","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Assembly of four modules onto a tetraazide platform by consecutive 1,2,3-triazole formations"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574095446812032","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Sequential “Click” – “Photo-Click” Cross-Linker for Catalyst-Free Ligation of Azide-Tagged Substrates"}]},{"@id":"https://cir.nii.ac.jp/crid/1360574096453620736","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chemoselective Layer-by-Layer Approach Utilizing Click Reactions with Ethynylcyclooctynes and Diazides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360576118754182272","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Azidoanilines by the Buchwald–Hartwig Amination"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658554489728","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Staudinger reaction using 2,6-dichlorophenyl azide derivatives for robust aza-ylide formation applicable to bioconjugation in living cells"}]},{"@id":"https://cir.nii.ac.jp/crid/1360848658564006400","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"A facile preparation of functional cycloalkynes <i>via</i> an azide-to-cycloalkyne switching approach"}]},{"@id":"https://cir.nii.ac.jp/crid/1360853567601909120","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"(Hexafluoroacetylacetonato)copper(<scp>i</scp>)–cycloalkyne complexes as protected cycloalkynes"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855568753877120","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recent Advances in Reactions of Azides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569310052096","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Ligand Behavior of a (<i>Z</i>)-Phosphazide (a 1,2,3,4λ<sup>5</sup>-Triazaphosphinine) and of the Corresponding Phosphazene (a 1,2λ<sup>5</sup>-Azaphosphete)"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569406154880","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Orthogonal dual-click diyne for CuAAC and/or SPAAC couplings"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569737606656","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Copper(I)-Catalyzed Three-Component Click/Alkynylation: One-Pot Synthesis of 5-Alkynyl-1,2,3-triazoles"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855569947108352","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Enhanced clickability of doubly sterically-hindered aryl azides"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570539256320","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Photoisomerizable Heterodienes Derived from a Phosphine Borane"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570939913600","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Bioorthogonal Reaction Pairs Enable Simultaneous, Selective, Multi‐Target Imaging"}]},{"@id":"https://cir.nii.ac.jp/crid/1360855570954805760","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Strain-Promoted [3 + 2] Azide−Alkyne Cycloaddition for Covalent Modification of Biomolecules in Living Systems"}]},{"@id":"https://cir.nii.ac.jp/crid/1360869855561325312","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Spot the difference in reactivity: a comprehensive review of site-selective multicomponent conjugation exploiting multi-azide compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044229621888","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Trifunctional Bis-azide Photoaffinity Probe"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044274482560","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Dendrimer design using CuI-catalyzed alkyne–azide “click-chemistry”"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137044293464320","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Dendrimers Clicked Together Divergently"}]},{"@id":"https://cir.nii.ac.jp/crid/1361137045736058880","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Multivalent glycoconjugate syntheses and applications using aromatic scaffolds"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418518786644992","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Mechanistic Investigation of the Staudinger Ligation"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418518901178880","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Highly accelerated inverse electron-demand cycloaddition of electron-deficient azides with aliphatic cyclooctynes"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418519669553920","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Heteroatom‐embedded Medium‐Sized Cycloalkynes: Concise Synthesis, Structural Analysis, and Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1361418520592651008","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Readily Accessible Bicyclononynes for Bioorthogonal Labeling and Three‐Dimensional Imaging of Living Cells"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993380801024","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"“Click” Dendrimers: Synthesis, Redox Sensing of Pd(OAc)<sub>2</sub>, and Remarkable Catalytic Hydrogenation Activity of Precise Pd Nanoparticles Stabilized by 1,2,3‐Triazole‐Containing Dendrimers"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699993500590848","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Thermodynamic Investigations of the Staudinger Reaction of Trialkylphosphines with 1-Adamantyl Azide and the Isolation of an Unusual s-cis Phosphazide"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995387227776","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Nuclear magnetic resonance studies. 6. Properties of phosphorus-nitrogen ylides"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699995649585408","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Discovery of new mutually orthogonal bioorthogonal cycloaddition pairs through computational screening"}]},{"@id":"https://cir.nii.ac.jp/crid/1361699996073370112","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Bioorthogonal Chemistry: Fishing for Selectivity in a Sea of Functionality"}]},{"@id":"https://cir.nii.ac.jp/crid/1361975843347550720","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Sequential conjugation methods based on triazole formation and related reactions using azides"}]},{"@id":"https://cir.nii.ac.jp/crid/1361975843352519424","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Facile assembly of three cycloalkyne-modules onto a platform compound bearing thiophene <i>S</i>,<i>S</i>-dioxide moiety and two azido groups"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981471295042688","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Metal-Free Sequential [3 + 2]-Dipolar Cycloadditions using Cyclooctynes and 1,3-Dipoles of Different Reactivity"}]},{"@id":"https://cir.nii.ac.jp/crid/1361981471415331328","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Design a Highly Reactive Trifunctional Core Molecule To Obtain Hyperbranched Polymers with over a Million Molecular Weight in One-Pot Click Polymerization"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262943335029888","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Perfluoroaryl Azide Staudinger Reaction: A Fast and Bioorthogonal Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944114277760","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Synthesis of Electron‐Rich Sterically Hindered P<sub>1</sub> Phosphazene Bases by the Staudinger Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944135026176","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Stepwise Huisgen Cycloaddition Process: Copper(I)-Catalyzed Regioselective “Ligation” of Azides and Terminal Alkynes"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944505925888","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Efficiency and Fidelity in a Click‐Chemistry Route to Triazole Dendrimers by the Copper(<scp>I</scp>)‐Catalyzed Ligation of Azides and Alkynes"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262944897970176","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Stabilised phosphazides"}]},{"@id":"https://cir.nii.ac.jp/crid/1362262945748891904","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"A Click Approach to Unprotected Glycodendrimers"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544418565599232","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Click–Click–Click: Single to Triple Modification of DNA"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544419284828544","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Relative Performance of Alkynes in Copper-Catalyzed Azide–Alkyne Cycloaddition"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544421256027648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"The Chemistry of Unusually Functionalized Azides"}]},{"@id":"https://cir.nii.ac.jp/crid/1362544421314834304","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Unexpected Staudinger reaction of α-azidoacetonitriles α-phenyl substituted with triphenylphosphine. Preparation, X-ray crystal and molecular structures of a phosphazine, an aminophosphonium carbanion salt and a phosphazide, with (Z)-configuration"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825893360935040","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Click Chemistry for Drug Development and Diverse Chemical–Biology Applications"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825893425763456","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Designing Miktoarm Polymers Using a Combination of “Click” Reactions in Sequence with Ring-Opening Polymerization"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894053277312","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Second-Generation Difluorinated Cyclooctynes for Copper-Free Click Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825894706461952","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Click Chemistry: Diverse Chemical Function from a Few Good Reactions"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825895666061440","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Strain-promoted double-click reaction for chemical modification of azido-biomolecules"}]},{"@id":"https://cir.nii.ac.jp/crid/1362825896191030144","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"1,3-Dipolar Cycloaddition Reactivities of Perfluorinated Aryl Azides with Enamines and Strained Dipolarophiles"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369001033600","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Visualizing Metabolically Labeled Glycoconjugates of Living Cells by Copper‐Free and Fast Huisgen Cycloadditions"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369219415040","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Organic Azides: An Exploding Diversity of a Unique Class of Compounds"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107369872655232","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chemoselective Formation of Successive Triazole Linkages in One Pot:  “Click−Click” Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1363107370972797568","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Rapid Cu-Free Click Chemistry with Readily Synthesized Biarylazacyclooctynones"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843542630528","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Selective Labeling of Living Cells by a Photo-Triggered Click Reaction"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388843940994560","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Structurally Diverse Dendritic Libraries:  A Highly Efficient Functionalization Approach Using Click Chemistry"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388844537157888","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Recent Advances in Recoverable Systems for the Copper-Catalyzed Azide-Alkyne Cycloaddition Reaction (CuAAC)"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388844551067520","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Click à la carte: robust semi-orthogonal alkyne protecting groups for multiple successive azide/alkyne cycloadditions"}]},{"@id":"https://cir.nii.ac.jp/crid/1363388846281913216","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Fine-Tuning Strain and Electronic Activation of Strain-Promoted 1,3-Dipolar Cycloadditions with Endocyclic Sulfamates in SNO-OCTs"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670318742174208","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Syntheses and Reactions of Polycationically Substituted Azido‐ and Diazidobenzenes"}]},{"@id":"https://cir.nii.ac.jp/crid/1363670320218141056","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Mechanism of Copper(I)-Catalyzed 5-Iodo-1,2,3-triazole Formation from Azide and Terminal Alkyne"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951794344014720","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Design and synthesis of a new macrobicyclic tris(phosphazide)"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795145791488","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Isomeric Cyclopropenes Exhibit Unique Bioorthogonal Reactivities"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795537286528","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Cyclopropenone-caged Sondheimer diyne (dibenzo[a,e]cyclooctadiyne): a photoactivatable linchpin for efficient SPAAC crosslinking"}]},{"@id":"https://cir.nii.ac.jp/crid/1363951795801186304","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Efficient Multigram Synthesis of the Repeating Unit of Gallic Acid-Triethylene Glycol Dendrimers"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233269022910976","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Chemoselective Sequential “Click” Ligation Using Unsymmetrical Bisazides"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233269816531840","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Diazo Compounds: Versatile Tools for Chemical Biology"}]},{"@id":"https://cir.nii.ac.jp/crid/1364233271221963648","@type":"Article","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Peptidotriazoles on Solid Phase:  [1,2,3]-Triazoles by Regiospecific Copper(I)-Catalyzed 1,3-Dipolar Cycloadditions of Terminal Alkynes to Azides"}]},{"@id":"https://cir.nii.ac.jp/crid/1390857280107647616","@type":"Article","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@language":"en","@value":"Development of Synthetic Chemistry on Organic Azides by Breaking their 1,3-Dipolar Characteristics"},{"@language":"ja","@value":"1,3-双極子としての性質を崩して展開する有機アジドの合成化学"}]},{"@id":"https://cir.nii.ac.jp/crid/1883679867625667328","@type":"Dataset","relationType":["isSupplementedBy"],"jpcoar:relatedTitle":[{"@value":"CCDC 1844604: Experimental Crystal Structure Determination"}]},{"@id":"https://cir.nii.ac.jp/crid/2050025942141183232","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Aromatic azido-selective reduction via the Staudinger reaction using tri-n-butylphosphonium tetrafluoroborate with triethylamine"}]},{"@id":"https://cir.nii.ac.jp/crid/2050588892097003008","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["isReferencedBy"],"jpcoar:relatedTitle":[{"@value":"Effect of resonance on the clickability of alkenyl azides in the strain-promoted cycloaddition with dibenzo-fused cyclooctynes"}]},{"@id":"https://cir.nii.ac.jp/crid/2050870367071328512","@type":"Article","resourceType":"学術雑誌論文(journal article)","relationType":["references"],"jpcoar:relatedTitle":[{"@value":"Sequential molecular conjugation using thiophene S,S-dioxides bearing a clickable functional group"}]}],"dataSourceIdentifier":[{"@type":"CROSSREF","@value":"10.1021/acs.orglett.8b01692"},{"@type":"KAKEN","@value":"PRODUCT-22400838"},{"@type":"KAKEN","@value":"PRODUCT-22356871"},{"@type":"KAKEN","@value":"PRODUCT-22212912"},{"@type":"KAKEN","@value":"PRODUCT-22209255"},{"@type":"OPENAIRE","@value":"doi_dedup___::88c8c0b1407a17cf5b07be6f0bc33b13"},{"@type":"CROSSREF","@value":"10.1039/c8cc09415b_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.3987/com-18-s(f)72_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d0cc06551j_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d0cc07212e_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d1qo01088c_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d1cc01143j_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.5059/yukigoseikyokaishi.80.1100_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.2c02895_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d0cc04606j_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1021/acs.orglett.4c00566_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.3389/fchem.2023.1237878_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/c8cc05791e_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1246/cl.190400_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d0cc07789e_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1021/acs.joc.1c02251_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/c9cc01113g_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d0cc05182a_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d4cc03359k_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/c9ob02698c_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"},{"@type":"CROSSREF","@value":"10.1039/d0cc01810d_references_DOI_JMjHSKHxxMYP7Bryg7ns2GwP0PO"}]}