Diastereoselective Ugi reaction of chiral 1,3-aminoalcohols derived from an organocatalytic Mannich reaction

Enantiomerically pure β-aminoalcohols, produced through an organocatalytic Mannich reaction, were subjected to an Ugi multicomponent reaction under classical or Lewis acid-promoted conditions with diastereoselectivities ranging from moderate to good. This approach represents a step-economical path t...

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Detalles Bibliográficos
Autores principales: Caputo, Samantha, Basso, Andrea, Moni, Lisa, Riva, Renata, Rocca, Valeria, Banfi, Luca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2016
Materias:
Letter
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734417/
https://www.ncbi.nlm.nih.gov/pubmed/26877816
http://dx.doi.org/10.3762/bjoc.12.15

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4734417/
https://www.ncbi.nlm.nih.gov/pubmed/26877816
http://dx.doi.org/10.3762/bjoc.12.15

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