Cargando…
Imine Reduction with Me(2)S-BH(3)
Although there exists a variety of different catalysts for hydroboration of organic substrates such as aldehydes, ketones, imines, nitriles etc., recent evidence suggests that tetra-coordinate borohydride species, formed by activation, redistribution, or decomposition of boron reagents, are the true...
Autores principales: | Kamal, Mohammad M., Liu, Zhizhou, Zhai, Siyuan, Vidović, Dragoslav |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8467297/ https://www.ncbi.nlm.nih.gov/pubmed/34576911 http://dx.doi.org/10.3390/molecules26185443 |
Ejemplares similares
-
An (R)‐Imine Reductase Biocatalyst for the Asymmetric Reduction of Cyclic Imines
por: Hussain, Shahed, et al.
Publicado: (2015) -
Engineering of Thermostable β‐Hydroxyacid Dehydrogenase for the Asymmetric Reduction of Imines
por: Stockinger, Peter, et al.
Publicado: (2020) -
Zn-Catalyzed Regioselective and Chemoselective Reduction of Aldehydes, Ketones and Imines
por: Zhang, Miaomiao, et al.
Publicado: (2022) -
Crystallographic characterization of (C(5)H(4)SiMe(3))(3)U(BH(4))
por: Windorff, Cory J., et al.
Publicado: (2021) -
Vancomycin-Iridium (III) Interaction: An Unexplored Route for Enantioselective Imine Reduction
por: Facchetti, Giorgio, et al.
Publicado: (2019)