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dc.contributor.authorJun, Joomyung V.
dc.contributor.authorRaines, Ronald T.
dc.date.accessioned2022-03-17T14:22:13Z
dc.date.available2022-03-16T18:06:45Z
dc.date.available2022-03-17T14:22:13Z
dc.date.issued2021-04
dc.date.submitted2021-03
dc.identifier.issn1523-7060
dc.identifier.issn1523-7052
dc.identifier.urihttps://hdl.handle.net/1721.1/141239.2
dc.description.abstractα-Aryl-α-diazoamides were synthesized in two steps under mild conditions. This expeditious route employs Pd-catalyzed C-H arylation of N-succinimidyl 2-diazoacetate to obtain N-succinimidyl 2-aryl-2-diazoacetates, followed by aminolysis. The ensuing diazo compounds can esterify carboxyl groups in aqueous solution, and the ester products are substrates for an esterase. The broad scope of the synthetic route enables the continued development of diazo compounds in chemical biology.en_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/acs.orglett.1c00793en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourcePMCen_US
dc.titleTwo-Step Synthesis of α-Aryl-α-diazoamides as Modular Bioreversible Labelsen_US
dc.typeArticleen_US
dc.identifier.citationJun, Joomyung V and Raines, Ronald T. 2021. "Two-Step Synthesis of α-Aryl-α-diazoamides as Modular Bioreversible Labels." Organic Letters, 23 (8).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemical Engineering
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MIT
dc.relation.journalOrganic Lettersen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-03-16T18:02:58Z
dspace.orderedauthorsJun, JV; Raines, RTen_US
dspace.date.submission2022-03-16T18:02:59Z
mit.journal.volume23en_US
mit.journal.issue8en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work Neededen_US


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