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dc.contributor.authorSagandira, Cloudius R.
dc.contributor.authorMathe, Francis M.
dc.contributor.authorGuyo, Upenyu
dc.contributor.authorWatts, Paul
dc.date.accessioned2021-05-12T08:33:42Z
dc.date.available2021-05-12T08:33:42Z
dc.date.issued2020
dc.identifier.issn404020
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/S0040402020306128
dc.identifier.urihttp://hdl.handle.net/11408/4163
dc.description.abstractInfluenza is a serious respiratory disease responsible for significant morbidity and mortality due to both annual epidemics and pandemics; its treatment involves the use of neuraminidase inhibitors. ( )-Oseltamivir phosphate (Tamiflu) approved in 1999, is one of the most potent oral anti-influenza neuraminidase inhibitors. Consequently, more than 70 Tamiflu synthetic procedures have been developed to date. Herein, we highlight the evolution of Tamiflu synthesis since its discovery over 20 years ago in the quest for a truly efficient, safe, cost-effective and environmentally benign synthetic procedure. We have selected a few representative routes to give a clear account of the past, present and the future with the advent of enabling technologies.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofseriesTetrahedron Volume 76, Issue 37;
dc.subjectEnabling technologiesen_US
dc.subjectEvolutionen_US
dc.subjectInfluenzaen_US
dc.subjectTamiflu synthesisen_US
dc.titleThe evolution of tamiflu synthesis, 20 years on: advent of enabling technologies the last piece of the puzzle?en_US
dc.typeArticleen_US
item.openairetypeArticle-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextWith Fulltext-
item.grantfulltextopen-
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