Investigations of the type ii intramolecular Diels-Alder reaction directed toward natural product synthesis

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Title

Investigations of the type ii intramolecular Diels-Alder reaction directed toward natural product synthesis

Content partner

University of Canterbury Library

Collection

UC Research Repository

Description

This thesis describes synthetic studies directed towards the total synthesis of the nakafuran and florlide marine natural products. Chapter One provides an overview of the importance of natural products to current medicinal chemistry and describes how the "supply issue" associated with these biologically derived compounds can be resolved through the process of total synthesis. Two families of marine natural products, the nakafurans and the florlides, are introduced as synthetic targets and st...

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Format

Research paper

Research format

Thesis

Thesis level

Doctoral

Date created

2006

Creator

Muscroft-Taylor, Andrew Clive

URL

http://hdl.handle.net/10092/1290

Related subjects

Type II Intramolecular Diels-Alder reaction / IMDA / T2IMDA / transition metal-catalysed cross-coupling / Stille / Negishi / Hydrostannylation / Enyne metathesis / Radical Fragmentation / Natural product synthesis / Nakafuran / Xenolide / Florlide / Bicyclo[4.3.1]decane / Bicyclo[4.3.1]decanone / Bicyclo[5.3.1]undecanone

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Copyright Andrew Clive Muscroft-Taylor

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