Rapid and Selective Electrophilic Trifluoromethylation of the 4,4-Difluoro-4-bora-3a,4a-diaza- s -indacene (BODIPY) Scaffold
✍ Scribed by Santschi, Nico; Cvengroš, Ján; Matthey, Coraline; Otth, Elisabeth; Antonio Togni, and
- Book ID
- 126603155
- Publisher
- John Wiley and Sons
- Year
- 2014
- Tongue
- English
- Weight
- 477 KB
- Volume
- 2014
- Category
- Article
- ISSN
- 1434-193X
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📜 SIMILAR VOLUMES
In the title compound, C 10 H 9 BF 2 N 2 , a boron-dipyrromethene (BODIPY) dye, a network of C-HÁ Á ÁF interactions help to establish the crystal packing. The asymmetric unit consists of two molecules.
The molecule of the title compound, C 15 H 10 BF 2 N 3 O 2 , is nonplanar; the benzene ring is twisted out of the borondipyrromethene mean plane with a dihedral angle of 57.0 (3) .
## Synthesis of 3,5-Diaryl-4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY r ) Dyes. -Condensation of arylpyrroles (IV), prepared via Suzuki coupling of arylboronic acids (II) to bromo pyrrole (I), gives highly colored dipyrrolemethenes (VI). Finally, addition of BF 3 -etherate leads to format