The title natural product 1 has been synthesized by treating the 1,2,3,5-tetrasubstituted pyrrole 23 with oxoperoxymolybdenum(pyridine) (hexamethylphosphoric triamide) (MoOPH). Compound 23 was itself prepared in seven steps from parent pyrrole using Ullmann-Goldberg and Suzuki-Miyaura cross-coupling, Vilsmeier-Haack formylation, electrophilic bromination, and Wittig olefination reactions as key steps. Related chemistry has been used to prepare discoipyrrole B (2).We thank the Australian Research Council and the Institute of Advanced Studies for financial support. Y.Z. gratefully acknowledges the China Scholarship Council for support
This thesis describes in detail our journey toward Maoecrystal V, a potential anti-cancer diterpenoi...
A total synthesis of the marine alkaloid discoipyrrole C (<b>3</b>) is described. In the pivotal ste...
The body of this thesis is comprised of four scientific journal articles and a patent. It is pr...
A total synthesis of the marine alkaloid discoipyrrole C (3) is described. In the pivotal step, the ...
Discoidin domain receptor 2 (DDR2) is a receptor tyrosine kinase involved in a variety of cellular r...
The replacement of the oil-based chemicals with those derived from biomasses is one of the most exci...
Previous work done by the Kerr group has shown that tetrahydro-1,2-oxazines can be efficiently synth...
Compounds containing the pyrrole ring as a core structural motif continue to show significant biolog...
In studies towards the synthesis of substituted pyrroles, the Knight group have adapted an aldol rea...
Compounds 1-6 and 11 representing key members of the marinoquinoline family of natural products, tog...
A one-step selective reaction was developed to synthesize a novel pyrrole family (20 different membe...
The biosynthesis of tetrapyrroles is briefly discussed and the important intermediates for chemical ...
The marine sponge-derived polyketide discodermolide is a potent antimitotic agent that represents a ...
The final examples in our ellipticine/pyrrolocarbazole synthesis programme are 7,10-dimethoxyellipti...
The following thesis contains three parts, where the common overall goal was to develop useful appli...
This thesis describes in detail our journey toward Maoecrystal V, a potential anti-cancer diterpenoi...
A total synthesis of the marine alkaloid discoipyrrole C (<b>3</b>) is described. In the pivotal ste...
The body of this thesis is comprised of four scientific journal articles and a patent. It is pr...
A total synthesis of the marine alkaloid discoipyrrole C (3) is described. In the pivotal step, the ...
Discoidin domain receptor 2 (DDR2) is a receptor tyrosine kinase involved in a variety of cellular r...
The replacement of the oil-based chemicals with those derived from biomasses is one of the most exci...
Previous work done by the Kerr group has shown that tetrahydro-1,2-oxazines can be efficiently synth...
Compounds containing the pyrrole ring as a core structural motif continue to show significant biolog...
In studies towards the synthesis of substituted pyrroles, the Knight group have adapted an aldol rea...
Compounds 1-6 and 11 representing key members of the marinoquinoline family of natural products, tog...
A one-step selective reaction was developed to synthesize a novel pyrrole family (20 different membe...
The biosynthesis of tetrapyrroles is briefly discussed and the important intermediates for chemical ...
The marine sponge-derived polyketide discodermolide is a potent antimitotic agent that represents a ...
The final examples in our ellipticine/pyrrolocarbazole synthesis programme are 7,10-dimethoxyellipti...
The following thesis contains three parts, where the common overall goal was to develop useful appli...
This thesis describes in detail our journey toward Maoecrystal V, a potential anti-cancer diterpenoi...
A total synthesis of the marine alkaloid discoipyrrole C (<b>3</b>) is described. In the pivotal ste...
The body of this thesis is comprised of four scientific journal articles and a patent. It is pr...