Enantioselective 1,3-Dipolar Cycloaddition Using (Z)-α-Amidonitroalkenes as a Key Step to the Access to Chiral cis-3,4-Diaminopyrrolidines †

The enantioselective 1,3-dipolar cycloaddition between imino esters and (Z)-nitroalkenes bearing a masked amino group in the β-position was studied using several chiral ligands and silver salts. The optimized reaction conditions were directly applied to the study of the scope of the reaction. The de...

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Detalles Bibliográficos
Autores principales: García-Mingüens, Eduardo, Ferrándiz-Saperas, Marcos, de Gracia Retamosa, M., Nájera, Carmen, Yus, Miguel, Sansano, José M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316397/
https://www.ncbi.nlm.nih.gov/pubmed/35889453
http://dx.doi.org/10.3390/molecules27144579

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9316397/
https://www.ncbi.nlm.nih.gov/pubmed/35889453
http://dx.doi.org/10.3390/molecules27144579

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