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Facile Deprotection of F-BODIPYs using Methylboronic Acid

dc.contributor.authorSmith, Craig D.
dc.contributor.authorThompson, Alison
dc.date.accessioned2020-06-22T16:25:40Z
dc.date.available2020-06-22T16:25:40Z
dc.date.issued2020
dc.description.abstract4,4-Difluoro-4-bora-3a,4a-diaza-s-indacenes (F-BODIPYs) are deprotected through removal of the –BF2 moiety upon treatment with methylboronic acid. The tolerance of various substitution patterns about the dipyrrinato core is demonstrated via the deprotection of thirteen F-BODIPYs and an F-aza-BODIPY. Work-up with aq. HBr affords the desired dipyrrin HBr salt in quantitative yield without need for purification.en_US
dc.identifier.urihttp://hdl.handle.net/10222/79417
dc.relation.ispartofRSC Advancesen_US
dc.titleFacile Deprotection of F-BODIPYs using Methylboronic Aciden_US
dc.typeArticleen_US

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