Skip navigation
Skip navigation

The Influence of Chiral Auxiliaries and Catalysts on the Selectivity of Intramolecular Conjugate Additions of Pyrrole to N -Tethered Michael Acceptors

Banwell, Martin; Beck, Daniel; Smith, Jason A

Description

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.

CollectionsANU Research Publications
Date published: 2004
Type: Journal article
URI: http://hdl.handle.net/1885/78363
Source: Organic and Biomolecular Chemistry
DOI: 10.1039/b312552a

Download

There are no files associated with this item.


Items in Open Research are protected by copyright, with all rights reserved, unless otherwise indicated.

Updated:  12 November 2018/ Responsible Officer:  University Librarian/ Page Contact:  Library Systems & Web Coordinator