ChemInform Abstract: Highly Enantioselective Aldol Reactions Using a tropos Dibenz[c,e]azepine Organocatalyst

A newly synthesized chiral primary tertiary diamine salt possessing a dibenz[c,e]azepine ring, promotes highly enantioselective crossed‐aldol reactions between cyclohexanone (I) and a series of aromatic aldehydes.

Gespeichert in:

Bibliographische Detailangaben
Veröffentlicht in:	ChemInform 2012-05, Vol.43 (19), p.no-no
Hauptverfasser:	Lygo, Barry, Davison, Christopher, Evans, Timothy, Gilks, James A. R., Leonard, John, Roy, Claude-Eric
Format:	Artikel
Sprache:	eng
Schlagworte:	C-C bond formation diastereoselective syntheses diastereoselective syntheses, enantioselective syntheses (incl. cis/trans‐isomerism) enantioselective syntheses (incl. cis/trans-isomerism)
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!

Beschreibung
Zusammenfassung:	A newly synthesized chiral primary tertiary diamine salt possessing a dibenz[c,e]azepine ring, promotes highly enantioselective crossed‐aldol reactions between cyclohexanone (I) and a series of aromatic aldehydes.
ISSN:	0931-7597 1522-2667
DOI:	10.1002/chin.201219041