Facile Deprotection of F-BODIPYs using Methylboronic Acid
| dc.contributor.author | Smith, Craig D. | |
| dc.contributor.author | Thompson, Alison | |
| dc.date.accessioned | 2020-06-22T16:25:40Z | |
| dc.date.available | 2020-06-22T16:25:40Z | |
| dc.date.issued | 2020 | |
| dc.identifier.uri | http://hdl.handle.net/10222/79417 | |
| dc.description.abstract | 4,4-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.relation.ispartof | RSC Advances | en_US |
| dc.title | Facile Deprotection of F-BODIPYs using Methylboronic Acid | en_US |
| dc.type | Article | en_US |
