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dc.contributor.authorAbularrage, Nile S
dc.contributor.authorLevandowski, Brian J
dc.contributor.authorGiancola, JoLynn B
dc.contributor.authorGraham, Brian J
dc.contributor.authorRaines, Ronald T
dc.date.accessioned2023-07-13T18:20:09Z
dc.date.available2023-07-13T18:20:09Z
dc.date.issued2023
dc.identifier.urihttps://hdl.handle.net/1721.1/151116
dc.description.abstract<jats:p>4<jats:italic>H</jats:italic>-Pyrazoles are emerging as useful click reagents.</jats:p>en_US
dc.language.isoen
dc.publisherRoyal Society of Chemistry (RSC)en_US
dc.relation.isversionof10.1039/D3CC00112Aen_US
dc.rightsCreative Commons Attribution-Noncommercialen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/en_US
dc.sourceRSCen_US
dc.titleBioorthogonal 4 H -pyrazole “click” reagentsen_US
dc.typeArticleen_US
dc.identifier.citationAbularrage, Nile S, Levandowski, Brian J, Giancola, JoLynn B, Graham, Brian J and Raines, Ronald T. 2023. "Bioorthogonal 4 H -pyrazole “click” reagents." Chemical Communications, 59 (30).
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistry
dc.relation.journalChemical Communicationsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2023-07-13T18:04:51Z
dspace.orderedauthorsAbularrage, NS; Levandowski, BJ; Giancola, JB; Graham, BJ; Raines, RTen_US
dspace.date.submission2023-07-13T18:04:53Z
mit.journal.volume59en_US
mit.journal.issue30en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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