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dc.contributor.authorRussell, M. Grace
dc.contributor.authorJamison, Timothy F
dc.date.accessioned2020-10-23T22:03:18Z
dc.date.available2020-10-23T22:03:18Z
dc.date.issued2019-06
dc.date.submitted2019-03
dc.identifier.issn1433-7851
dc.identifier.issn1521-3773
dc.identifier.urihttps://hdl.handle.net/1721.1/128199
dc.description.abstractHerein, the blockbuster antibacterial drug linezolid is synthesized from simple starting blocks by a convergent continuous flow sequence involving seven (7) chemical transformations. This is the highest total number of distinct reaction steps ever performed in continuous flow without conducting solvent exchanges or intermediate purification. Linezolid was obtained in 73 % isolated yield in a total residence time of 27 minutes, corresponding to a throughput of 816 mg h[superscript −1].en_US
dc.description.sponsorshipDefense Advanced Research Projects Agency (Grant N66001-16-C-4005)en_US
dc.publisherWileyen_US
dc.relation.isversionofhttp://dx.doi.org/10.1002/anie.201901814en_US
dc.rightsCreative Commons Attribution-Noncommercial-Share Alikeen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/en_US
dc.sourceProf. Jamisonen_US
dc.titleSeven‐Step Continuous Flow Synthesis of Linezolid Without Intermediate Purificationen_US
dc.typeArticleen_US
dc.identifier.citationRussell, M. Grace and Timothy F Jamison. "Seven‐Step Continuous Flow Synthesis of Linezolid Without Intermediate Purification." Angewandte Chemie 58, 23 (June 2019): 7678-7681en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.relation.journalAngewandte Chemie - International Editionen_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
dspace.date.submission2020-10-20T21:30:06Z
mit.journal.volume58en_US
mit.journal.issue23en_US
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusComplete


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