Enantio- and regioselective iridium-catalyzed allylic esterification

A highly enantioselective and regioselective Ir-catalyzed allylic esterification is described, in which branched allylic esters are synthesized directly. Carboxylates were used as nucleophiles and linear allylic phosphates as electrophiles. In some cases the allylic substitution reaction was found t...

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Hauptverfasser: Qu, Jianping (VerfasserIn) , Roßberg, Lydia (VerfasserIn) , Helmchen, Günter (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: January 14, 2014
In: Journal of the American Chemical Society
Year: 2014, Jahrgang: 136, Heft: 4, Pages: 1272-1275
ISSN:1520-5126
DOI:10.1021/ja411869r
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1021/ja411869r
Verlag, lizenzpflichtig, Volltext: https://pubs.acs.org/doi/10.1021/ja411869r
Volltext
Verfasserangaben:Jianping Qu, Lydia Roßberg, and Günter Helmchen
Beschreibung
Zusammenfassung:A highly enantioselective and regioselective Ir-catalyzed allylic esterification is described, in which branched allylic esters are synthesized directly. Carboxylates were used as nucleophiles and linear allylic phosphates as electrophiles. In some cases the allylic substitution reaction was found to be accompanied by a kinetic resolution process, which causes a change of the enantiomeric excess.
Beschreibung:Gesehen am 12.10.2020
Beschreibung:Online Resource
ISSN:1520-5126
DOI:10.1021/ja411869r