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Highly Diastereo- and Enantioselective Synthesis of alpha-Spiro-delta-lactams by an Organocascade Reaction

Publikace na Přírodovědecká fakulta |
2017

Tento text není v aktuálním jazyce dostupný. Zobrazuje se verze "en".Abstrakt

An asymmetric synthesis of alpha-spiro-delta-lactams by an organocascade reaction of easily accessible starting materials has been accomplished. The catalytic sequence begins with enantioselective Michael addition of a beta-ketoamide to an a, alpha,beta-unsaturated aldehyde, catalyzed by a secondary amine catalyst, and is followed by hemiaminal annulation.

Optically enantiopure compounds with three stereogenic centres are obtained in good yields and excellent selectivities (up to > 20:1 dr and up to > 99 % ee).