Cargando…
Nitroso Diels-Alder Cycloadducts Derived From N-Acyl-1,2-dihydropyridines as a New Platform to Molecular Diversity
This review focuses upon the use of nitroso Diels–Alder reactions as a structural complexity generating reaction that has been so far a quite scarcely treated topic, despite its potential. In particular, the use of N-acyl-1,2-dihydropyridines as a non-symmetrical diene component in nitroso Diels–Ald...
Autores principales: | Menichetti, Andrea, Berti, Francesco, Pineschi, Mauro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7038088/ https://www.ncbi.nlm.nih.gov/pubmed/32012951 http://dx.doi.org/10.3390/molecules25030563 |
Ejemplares similares
-
Alternating Current Electrolysis as Efficient Tool for the Direct Electrochemical Oxidation of Hydroxamic Acids for Acyl Nitroso Diels–Alder Reactions
por: Fährmann, Jan, et al.
Publicado: (2021) -
Peroxidase-induced C–N bond formation via nitroso ene and Diels–Alder reactions
por: Jäger, Christina, et al.
Publicado: (2023) -
Stereo- and regioselectivity of the hetero-Diels–Alder reaction of nitroso derivatives with conjugated dienes
por: Brulíková, Lucie, et al.
Publicado: (2016) -
Hetero‐Diels–Alder Cycloaddition with RAFT Polymers as Bioconjugation Platform
por: Beloqui, Ana, et al.
Publicado: (2020) -
The hexadehydro-Diels–Alder reaction
por: Hoye, Thomas R., et al.
Publicado: (2012)