| dc.contributor.author | Lundrigan, Travis | en_US |
| dc.contributor.author | Thompson, Alison | en_US |
| dc.date.accessioned | 2013-08-12T17:55:00Z | |
| dc.date.available | 2013-08-12T17:55:00Z | |
| dc.date.issued | 2013-01 | en_US |
| dc.identifier.citation | Lundrigan, Travis, and Alison Thompson. 2013. "Conversion of F-BODIPYs to Cl-BODIPYs: Enhancing the Reactivity of F-BODIPYs." Journal of Organic Chemistry 78(2): 757-761. | en_US |
| dc.identifier.issn | 0022-3263 | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1021/jo302277d | en_US |
| dc.identifier.uri | http://hdl.handle.net/10222/30714 | |
| dc.description.abstract | A new method for the synthesis of Cl-BODIPYs from F-BODIPYs is reported, merely requiring
treatment of the F-BODIPY with boron trichloride. Cl-BODIPYs are exploited as synthetic
intermediates generated in situ for the overall conversion of F-BODIPYs to O- and C-BODIPYs in high
overall yields using a mild one-pot procedure. This route enables F-BODIPYs to be transformed into
derivatives that are not accessible via the direct route, as demonstrated via the use of
1,3-propanediol. | en_US |
| dc.relation.ispartof | Journal of Organic Chemistry | en_US |
| dc.title | Conversion of F-BODIPYs to Cl-BODIPYs: Enhancing the Reactivity of F-BODIPYs | en_US |
| dc.type | article | en_US |
| dc.identifier.volume | 78 | en_US |
| dc.identifier.issue | 2 | en_US |
| dc.identifier.startpage | 757 | en_US |
