The Influence of Chiral Auxiliaries and Catalysts on the Selectivity of Intramolecular Conjugate Additions of Pyrrole to N -Tethered Michael Acceptors
A series of pyrroles incorporating N-tethered acrylates and related groups has been prepared and examined for their capacity to undergo intramolecular Michael addition reactions to form, in a diastereo- or enantio-selective fashion, the corresponding 8-substituted tetrahydroindolizidine or homologues thereof.
|Collections||ANU Research Publications|
|Source:||Organic and Biomolecular Chemistry|
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