Cargando…
Multi-Gram Synthesis of Enantiopure 1,5-Disubstituted Tetrazoles Via Ugi-Azide 3-Component Reaction
Tetrazoles have been widely studied for their biological properties. An efficient route for large-scale synthesis of 1,5-disubstituted tetrazoles (1,5-DTs) is presented. The strategy exploits a reductive approach to synthetize a cyclic chiral imine substrate which is then converted into the target p...
Autores principales: | Capurro, Pietro, Moni, Lisa, Galatini, Andrea, Mang, Christian, Basso, Andrea |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278549/ https://www.ncbi.nlm.nih.gov/pubmed/30366358 http://dx.doi.org/10.3390/molecules23112758 |
Ejemplares similares
-
Consecutive hydrazino-Ugi-azide reactions: synthesis of acylhydrazines bearing 1,5-disubstituted tetrazoles
por: Barreto, Angélica de Fátima S, et al.
Publicado: (2017) -
Synthesis of Novel bis-1,5-Disubstituted-1H-Tetrazoles by an Efficient Catalyst-Free Ugi-Azide Repetitive Process
por: Cárdenas-Galindo, Luís E., et al.
Publicado: (2015) -
Combining the Ugi-azide multicomponent reaction and rhodium(III)-catalyzed annulation for the synthesis of tetrazole-isoquinolone/pyridone hybrids
por: Ojeda, Gerardo M, et al.
Publicado: (2019) -
Enantioselective Ugi and Ugi-azide reactions catalyzed by anionic stereogenic-at-cobalt(III) complexes
por: Sun, Bing-Bing, et al.
Publicado: (2022) -
Exploitation of the Ugi 5-Center-4-Component Reaction (U-5C-4CR) for the Generation of Diverse Libraries of Polycyclic (Spiro)Compounds
por: Moni, Lisa, et al.
Publicado: (2018)