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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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מידע ביבליוגרפי
Principais autores: Samantha Caputo, Andrea Basso, Lisa Moni, Renata Riva, Valeria Rocca, Luca Banfi
פורמט: Artigo
שפה:Inglês
יצא לאור: Beilstein-Institut 2016-01-01
סדרה:Beilstein Journal of Organic Chemistry
נושאים:
גישה מקוונת:https://doi.org/10.3762/bjoc.12.15
תגים: הוספת תג
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