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dc.contributor.authorFu, Wai Chung
dc.contributor.authorJamison, Timothy F
dc.date.accessioned2020-06-23T19:37:48Z
dc.date.available2020-06-23T19:37:48Z
dc.date.issued2019-07
dc.identifier.issn1523-7052
dc.identifier.urihttps://hdl.handle.net/1721.1/125954
dc.description.abstractA modular continuous flow synthesis of imatinib and analogues is reported. Structurally diverse imatinib analogues are rapidly generated using three readily available building blocks via a flow hydration/chemoselective C-N coupling sequence. The newly developed continuous flow hydration and amidation modules each exhibit a broad scope with good to excellent yields. Overall, the method described does not require solvent switches, in-line purifications, or packed-bed apparatuses due to the judicious manipulation of flow setups and solvent mixtures.en_US
dc.description.sponsorshipDARPA (contract no. ARO W911NF-16-2-0023)en_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionof10.1021/ACS.ORGLETT.9B02259en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceOther repositoryen_US
dc.titleModular continuous flow synthesis of imatinib and analoguesen_US
dc.typeArticleen_US
dc.identifier.citationFu, Wai Chung, and Timothy F. Jamison, "Modular continuous flow synthesis of imatinib and analogues." Organic Letters 21, 15 (July 2019): p. 6112-16 doi 10.1021/ACS.ORGLETT.9B02259 ©2019 Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
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.updated2019-12-18T17:55:25Z
dspace.date.submission2019-12-18T17:55:27Z
mit.journal.volume21en_US
mit.journal.issue15en_US
mit.licensePUBLISHER_POLICY
mit.metadata.statusComplete


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