Abstract
Supported reagents and scavengers have become key tools for the synthesis of biologically important molecular entities. The complexity of the target molecules attainable and the synthetic flexibility afforded by these systems now rivals any solution phase approach whilst offering the added advantage of rapid purification and work-up. This short review highlights the application of these immobilized reagents to the preparation of alkaloid natural products.
Keywords: organic synthesis, purification techniques, reagent immobilization, amaryllidaceae alkaloids, nornicotine, polymer-supported carbonate, trifluoroacetamide
Current Organic Chemistry
Title: Synthesis of Alkaloid Natural Products Using Solid-Supported Reagents and Scavengers
Volume: 9 Issue: 15
Author(s): I. R. Baxendale and S. V. Ley
Affiliation:
Keywords: organic synthesis, purification techniques, reagent immobilization, amaryllidaceae alkaloids, nornicotine, polymer-supported carbonate, trifluoroacetamide
Abstract: Supported reagents and scavengers have become key tools for the synthesis of biologically important molecular entities. The complexity of the target molecules attainable and the synthetic flexibility afforded by these systems now rivals any solution phase approach whilst offering the added advantage of rapid purification and work-up. This short review highlights the application of these immobilized reagents to the preparation of alkaloid natural products.
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Cite this article as:
Baxendale R. I. and Ley V. S., Synthesis of Alkaloid Natural Products Using Solid-Supported Reagents and Scavengers, Current Organic Chemistry 2005; 9 (15) . https://dx.doi.org/10.2174/138527205774370513
DOI https://dx.doi.org/10.2174/138527205774370513 |
Print ISSN 1385-2728 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5348 |
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Catalytic C-H bond activation as a tool for functionalization of heterocycles
The major topic is the functionalization of heterocycles through catalyzed C-H bond activation. The strategies based on C-H activation not only provide straightforward formation of C-C or C-X bonds but, more importantly, allow for the avoidance of pre-functionalization of one or two of the cross-coupling partners. The beneficial impact of ...read more
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