4-4-difluoro-4-bora-3a-4a-diaza-s-indacene and boron-trichloride

4-4-difluoro-4-bora-3a-4a-diaza-s-indacene has been researched along with boron-trichloride* in 1 studies

Other Studies

1 other study(ies) available for 4-4-difluoro-4-bora-3a-4a-diaza-s-indacene and boron-trichloride

Article	Year
Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the reactivity of F-BODIPYs. The Journal of organic chemistry, 2013, Jan-18, Volume: 78, Issue:2 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. Topics: Boranes; Boron Compounds; Chlorides; Crystallography, X-Ray; Fluorescent Dyes; Molecular Structure; Propylene Glycols	2013

Article

Year

Conversion of F-BODIPYs to Cl-BODIPYs: enhancing the reactivity of F-BODIPYs.

The Journal of organic chemistry, 2013, Jan-18, Volume: 78, Issue:2

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.

Topics: Boranes; Boron Compounds; Chlorides; Crystallography, X-Ray; Fluorescent Dyes; Molecular Structure; Propylene Glycols

2013