Cargando…
MIDA boronates are hydrolysed fast and slow by two different mechanisms
MIDA boronates (N-methylimidodiacetic boronic acid esters) serve as an increasingly general platform for building-block-based small molecule construction, largely due to the dramatic and general rate differences with which they are hydrolysed under various basic conditions. Yet the mechanistic under...
Autores principales: | Gonzalez, Jorge A., Ogba, O. Maduka, Morehouse, Gregory F., Rosson, Nicholas, Houk, Kendall N., Leach, Andrew G., Cheong, Paul H.-Y., Burke, Martin D., Lloyd-Jones, Guy C. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5115273/ https://www.ncbi.nlm.nih.gov/pubmed/27768100 http://dx.doi.org/10.1038/nchem.2571 |
Ejemplares similares
-
MIDA boronate allylation – synthesis of ibuprofen
por: Phillips, David, et al.
Publicado: (2020) -
A Convenient, Rapid, Conventional Heating Route to MIDA Boronates
por: McGown, Andrew, et al.
Publicado: (2022) -
Regioselective Electrophilic Addition to Propargylic B(MIDA)s Enabled by β‐Boron Effect
por: Li, Yin, et al.
Publicado: (2023) -
meta-Selective C–H functionalisation of aryl boronic acids directed by a MIDA-derived boronate ester
por: Williams, Alexander F., et al.
Publicado: (2020) -
Oxidative Heck Reactions using Aryltrifluoroborates and Aryl N-Methyliminodiacetic Acid (MIDA) Boronates
por: Sävmarker, Jonas, et al.
Publicado: (2012)