Enantioselective preparation of 1(R)-hydroxypolygodial (5) has been achieved starting from alpha-ionone through a synthetic strategy involving a Corey-Bakshi-Shibata oxazaborolidine-mediated reduction and a stereoselective Diels-Alder reaction as key steps.
Titolo: | Enantioselective synthesis of 1 (R)-hydroxypolygodial |
Autori: | |
Data di pubblicazione: | 2005 |
Rivista: | |
Abstract: | Enantioselective preparation of 1(R)-hydroxypolygodial (5) has been achieved starting from alpha-ionone through a synthetic strategy involving a Corey-Bakshi-Shibata oxazaborolidine-mediated reduction and a stereoselective Diels-Alder reaction as key steps. |
Handle: | http://hdl.handle.net/11386/1058614 |
Appare nelle tipologie: | 1.1.2 Articolo su rivista con ISSN |
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