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dc.contributor.authorZiegler, Robert E.
dc.contributor.authorDesai, Bimbisar K.
dc.contributor.authorJee, Jo-Ann
dc.contributor.authorGupton, B. Frank
dc.contributor.authorRoper, Thomas D.
dc.contributor.authorJamison, Timothy F
dc.date.accessioned2020-06-23T19:06:21Z
dc.date.available2020-06-23T19:06:21Z
dc.date.issued2018-06
dc.identifier.issn1521-3773
dc.identifier.urihttps://hdl.handle.net/1721.1/125949
dc.description.abstractDolutegravir (DTG), an important active pharmaceutical ingredient (API) used in combination therapy for the treatment of HIV, has been synthesized in continuous flow. By adapting the reported GlaxoSmithKline process chemistry batch route for Cabotegravir, DTG was produced in 4.5 h in sequential flow operations from commercially available materials. Key features of the synthesis include rapid manufacturing time for pyridone formation, one-step direct amidation of a functionalized pyridone, and telescoping of multiple steps to avoid isolation of intermediates and enable for greater throughput.en_US
dc.language.isoen
dc.publisherWileyen_US
dc.relation.isversionof10.1002/ANIE.201802256en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceWileyen_US
dc.title7-step flow synthesis of the HIV integrase inhibitor Dolutegraviren_US
dc.typeArticleen_US
dc.identifier.citationZiegler, Robert E., et al., "7-step flow synthesis of the HIV integrase inhibitor Dolutegravir." Angewandte Chemie International Edition 57, 24 (June 2018): p. 7181-85 doi 10.1002/ANIE.201802256 ©2018 Author(s)en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.relation.journalAngewandte Chemie International Editionen_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.updated2019-12-18T17:02:26Z
dspace.date.submission2019-12-18T17:02:28Z
mit.journal.volume57en_US
mit.journal.issue24en_US
mit.metadata.statusComplete


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