This thesis examines the total synthesis of the macroline-related indole alkaloid alstonerine and related compounds. It is divided into three sections: The first section provides a review of the total synthesis efforts reported by Cook, Martin, Kuethe, and Kwon, as well previous work within the Craig group. The second section discusses the results of our investigations. The optimisation of the synthesis of key intermediate α,β-unsaturated lactam alcohol via directed-aziridine ring-opening is presented in detail. Our progress towards the synthesis of macroline-related alkaloids macroline, alstolactone, anhydromacrosalhine-methine and alstonerinal, as well as their N4-tosyl derivatives, from the key intermediate is discussed. The findings f...
This thesis describes the attempted syntheses of polyamine based peptide toxins (enzymatically) and ...
Due to their extensive and important medicinal properties, the indole alkaloids are an important cla...
This thesis describes our efforts towards the total synthesis of natural products and the developmen...
The work presented in this thesis focuses on the synthesis of monoterpene indole alkaloids. The fir...
Graduation date: 1988A formal total synthesis of the macrolactone pyrolizidine alkaloid (-)-integerr...
This thesis is divided into three chapters. Chapter 1 provides brief reviews on the subjects of pre...
A total synthesis of the racemic modification, (±)-2, of the tazettine-type alkaloid 3-O-demethylmac...
ABSTRACT: A detailed account of the development of a general strategy for synthesis of the C-19 meth...
This thesis is divided into three chapters. Chapter 1 provides brief reviews on the subjects of prev...
This thesis covers three areas of research relating to pyrrolizidine alkaloids, (a) Synthesis of mac...
Synthetic studies towards the total synthesis of the macrocyclic marine alkaloid ‘upenamide (I) are ...
This thesis is divided into three sections. Section one is a review of recent progress in the synthe...
Rapid synthesis of the pentacyclic core structure of macroline-type indole alkaloids, and its applic...
Includes bibliographical references.This thesis begins with a review (Chapter 1) of methodologies fo...
The (7R)-sarpagine/macroline related oxindole alkaloids (-)-isoalstonisine (27) and (-)-macrogentine...
This thesis describes the attempted syntheses of polyamine based peptide toxins (enzymatically) and ...
Due to their extensive and important medicinal properties, the indole alkaloids are an important cla...
This thesis describes our efforts towards the total synthesis of natural products and the developmen...
The work presented in this thesis focuses on the synthesis of monoterpene indole alkaloids. The fir...
Graduation date: 1988A formal total synthesis of the macrolactone pyrolizidine alkaloid (-)-integerr...
This thesis is divided into three chapters. Chapter 1 provides brief reviews on the subjects of pre...
A total synthesis of the racemic modification, (±)-2, of the tazettine-type alkaloid 3-O-demethylmac...
ABSTRACT: A detailed account of the development of a general strategy for synthesis of the C-19 meth...
This thesis is divided into three chapters. Chapter 1 provides brief reviews on the subjects of prev...
This thesis covers three areas of research relating to pyrrolizidine alkaloids, (a) Synthesis of mac...
Synthetic studies towards the total synthesis of the macrocyclic marine alkaloid ‘upenamide (I) are ...
This thesis is divided into three sections. Section one is a review of recent progress in the synthe...
Rapid synthesis of the pentacyclic core structure of macroline-type indole alkaloids, and its applic...
Includes bibliographical references.This thesis begins with a review (Chapter 1) of methodologies fo...
The (7R)-sarpagine/macroline related oxindole alkaloids (-)-isoalstonisine (27) and (-)-macrogentine...
This thesis describes the attempted syntheses of polyamine based peptide toxins (enzymatically) and ...
Due to their extensive and important medicinal properties, the indole alkaloids are an important cla...
This thesis describes our efforts towards the total synthesis of natural products and the developmen...