Cargando…
Borylation Directed Borylation of Indoles Using Pyrazabole Electrophiles: A One‐Pot Route to C7‐Borylated‐Indolines
Pyrazabole (1) is a readily accessible diboron compound that can be transformed into ditopic electrophiles. In 1 (and derivatives), the B⋅⋅⋅B separation is ca. 3 Å, appropriate for one boron centre bonding to N and one to the C7 of indoles and indolines. This suitable B⋅⋅⋅B separation enables double...
Autores principales: | Pahl, Jürgen, Noone, Emily, Uzelac, Marina, Yuan, Kang, Ingleson, Michael J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401042/ https://www.ncbi.nlm.nih.gov/pubmed/35686751 http://dx.doi.org/10.1002/anie.202206230 |
Ejemplares similares
-
Borylation directed borylation of N-alkyl anilines using iodine activated pyrazaboles
por: Millet, C. R. P., et al.
Publicado: (2023) -
Synthesis
of Electrophiles Derived from Dimeric Aminoboranes
and Assessing Their Utility in the Borylation of π Nucleophiles
por: Millet, Clément R. P., et al.
Publicado: (2022) -
Amides as modifiable directing groups in electrophilic borylation
por: Iqbal, Saqib A., et al.
Publicado: (2023) -
Acyl‐Directed ortho‐Borylation of Anilines and C7 Borylation of Indoles using just BBr(3)
por: Iqbal, Saqib A., et al.
Publicado: (2019) -
A modular route to boron doped PAHs by combining borylative cyclisation and electrophilic C–H borylation
por: Crossley, D. L., et al.
Publicado: (2017)