Cargando…
Unveiling the Stereoselectivity and Regioselectivity of the [3+2] Cycloaddition Reaction between N-methyl-C-4-methylphenyl-nitrone and 2-Propynamide from a MEDT Perspective
[3+2] cycloaddition reactions play a crucial role in synthesizing complex organic molecules and have significant applications in drug discovery and materials science. In this study, the [3+2] cycloaddition (32CA) reactions of N-methyl-C-4-methyl phenyl-nitrone 1 and 2-propynamide 2, which have not b...
Autores principales: | Salih, Sabir A. Mohammed, Basheer, Huda A., de Julián-Ortiz, Jesus Vicente, Mohammad-Salim, Haydar A. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10218864/ https://www.ncbi.nlm.nih.gov/pubmed/37240445 http://dx.doi.org/10.3390/ijms24109102 |
Ejemplares similares
-
Understanding the Molecular Mechanism of the Rearrangement of Internal Nitronic Ester into Nitronorbornene in Light of the MEDT Study
por: Kącka-Zych, Agnieszka
Publicado: (2019) -
N-Benzyl-2-propynamide
por: Chen, Mei-Mei, et al.
Publicado: (2009) -
Full Regio- and Stereoselective Protocol for the Synthesis of New Nicotinoids via Cycloaddition Processes with the Participation of Trans-Substituted Nitroethenes: Comprehensive Experimental and MEDT Study
por: Kras, Jowita, et al.
Publicado: (2023) -
Predicting reactivity for bioorthogonal cycloadditions involving nitrones
por: Nakajima, Masaya, et al.
Publicado: (2020) -
Understanding the different reactivity of (Z)- and (E)-β-nitrostyrenes in [3+2] cycloaddition reactions. An MEDT study
por: Ríos-Gutiérrez, Mar, et al.
Publicado: (2021)