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Preparation of some angularly substituted and highly functionalized quinolizidines as building blocks for the synthesis of various alkaloids and related scaffolds of medicinal interest
Citation
Bissember, AC and Banwell, MG, Preparation of some angularly substituted and highly functionalized quinolizidines as building blocks for the synthesis of various alkaloids and related scaffolds of medicinal interest, Tetrahedron, 65, (39) pp. 8222-8230. ISSN 0040-4020 (2009) [Refereed Article]
Copyright Statement
Copyright 2009 Elsevier
DOI: doi:10.1016/j.tet.2009.07.067
Abstract
The epimeric forms of the angularly substituted quinolizidine 6, representing potentially useful building
blocks for the synthesis of various alkaloids, have been prepared via a pathway involving two consecutive
ring-closing metathesis reactions. Variously hydroxy-protected derivatives (21, 22, and 26–29) of these
compounds have also been generated.
Item Details
| Item Type: | Refereed Article |
|---|---|
| Keywords: | Alkaloids; Fasicularin; Quinolizidines; Ring-closing metathesis; Vinylation |
| Research Division: | Chemical Sciences |
| Research Group: | Organic chemistry |
| Research Field: | Organic chemical synthesis |
| Objective Division: | Expanding Knowledge |
| Objective Group: | Expanding knowledge |
| Objective Field: | Expanding knowledge in the chemical sciences |
| UTAS Author: | Bissember, AC (Associate Professor Alex Bissember) |
| ID Code: | 85974 |
| Year Published: | 2009 |
| Web of Science® Times Cited: | 6 |
| Deposited By: | Chemistry |
| Deposited On: | 2013-08-19 |
| Last Modified: | 2015-02-13 |
| Downloads: | 0 |
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