Asymmetric Aldol Reaction of α,α-Disubstituted Acetaldehydes Catalyzed by Diphenylprolinol Silyl Ether for the Construction of Quaternary Stereogenic Centers

The asymmetric cross‐aldol reaction of α,α‐disubstituted acetaldehydes with commercial ethyl glyoxylate polymer was successfully catalyzed by diphenylprolinol silyl ether 3 to generate all‐carbon quaternary stereogenic centers with good enantioselectivity. Diphenylprolinol silyl ether is an effectiv...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of organic chemistry 2015-07, Vol.2015 (20), p.4316-4319
Hauptverfasser: Hayashi, Yujiro, Shomura, Hiroki, Xu, Qianqian, Lear, Martin J., Sato, Itaru
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The asymmetric cross‐aldol reaction of α,α‐disubstituted acetaldehydes with commercial ethyl glyoxylate polymer was successfully catalyzed by diphenylprolinol silyl ether 3 to generate all‐carbon quaternary stereogenic centers with good enantioselectivity. Diphenylprolinol silyl ether is an effective organocatalyst in the asymmetric cross‐aldol reaction of α,α‐disubstituted acetaldehydes with commercial ethyl glyoxylate polymer to generate all‐carbon quaternary stereogenic centers with good enantioselectivity.
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.201500585