Cargando…
Ortho-Phosphinoarenesulfonamide-Mediated Staudinger Reduction of Aryl and Alkyl Azides
Conventional Staudinger reductions of organic azides are sluggish with aryl or bulky aliphatic azides. In addition, Staudinger reduction usually requires a large excess of water to promote the decomposition of the aza-ylide intermediate into phosphine oxide and amine products. To overcome the challe...
Autores principales: | Li, Xingzhuo, Wang, Zhenguo, Luo, Wenjun, Wang, Zixu, Yin, Keshu, Li, Le |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9458194/ https://www.ncbi.nlm.nih.gov/pubmed/36080474 http://dx.doi.org/10.3390/molecules27175707 |
Ejemplares similares
-
Ortho-Nitro Effect on the Diastereoselective Control in Sulfa-Staudinger and Staudinger Cycloadditions
por: Yang, Zhanhui, et al.
Publicado: (2017) -
Short and Efficient Synthesis of Alkyl- and Aryl-Ortho-Hydroxy-Anilides and their Antibiotic Activity
por: Krauß, Jürgen, et al.
Publicado: (2014) -
Site‐Selective C−H Arylation of Diverse Arenes Ortho to Small Alkyl Groups
por: Dhankhar, Jyoti, et al.
Publicado: (2022) -
Small Molecule Control of Protein Function through Staudinger Reduction
por: Luo, Ji, et al.
Publicado: (2016) -
Convenient Entry to (18)F‐Labeled Amines through the Staudinger Reduction
por: Stéen, E. Johanna L., et al.
Publicado: (2019)