A comprehensive synthetic review of the pederin family of cytotoxins, including pederin, the mycalamides, and psymberin, is presented. A number of approaches to the synthesis of these molecules is covered, including pederic acid, the tetrahydropyranyl ring of pederin, the trioxadecalin ring of the mycalamides, and psymberin fragments. Coupling strategies for these compounds are also summarized. An overview of biological activity at various positions of mycalamide A, as well as some analogs, is given
This thesis describes the development of methods and strategies inspired by three natural products: ...
Three aspects of the protecting-group-free (PGF) synthesis of small molecules have been described in...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...
An investigation of the pederin family of natural products has led to the total synthesis of theoped...
Abstract — Pederin, the vesicant component found in the haemolymph of many species of the staphylini...
The electron transfer initiated cyclization (ETIC) has been shown to be an efficient method for the ...
Mycalamides A and B, isolated recently from a marine sponge of the genus Mycale, show strong in vitr...
As an alternative to our earlier synthesis of Pederin (1) we have investigated a new strategy based ...
This thesis details the optimisation and development to the synthesis of the ABC fragment of pecteno...
This thesis details the optimisation and development to the synthesis of the ABC fragment of pecteno...
Two synthetic approaches to psymberin have been accomplished. A highly convergent first generation s...
The pyrrolidine nucleus is found in many biologically important natural products. This dissertation ...
This thesis details the application of two synthetic methodologies, developed by the Donohoe group, ...
In this thesis, synthetic chemistry was used as a tool in the exploration of various aspects of natu...
The cobalt-catalysed oxidative cyclisation of 5-hydroxy alkenes has been demonstrated to be a powerf...
This thesis describes the development of methods and strategies inspired by three natural products: ...
Three aspects of the protecting-group-free (PGF) synthesis of small molecules have been described in...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...
An investigation of the pederin family of natural products has led to the total synthesis of theoped...
Abstract — Pederin, the vesicant component found in the haemolymph of many species of the staphylini...
The electron transfer initiated cyclization (ETIC) has been shown to be an efficient method for the ...
Mycalamides A and B, isolated recently from a marine sponge of the genus Mycale, show strong in vitr...
As an alternative to our earlier synthesis of Pederin (1) we have investigated a new strategy based ...
This thesis details the optimisation and development to the synthesis of the ABC fragment of pecteno...
This thesis details the optimisation and development to the synthesis of the ABC fragment of pecteno...
Two synthetic approaches to psymberin have been accomplished. A highly convergent first generation s...
The pyrrolidine nucleus is found in many biologically important natural products. This dissertation ...
This thesis details the application of two synthetic methodologies, developed by the Donohoe group, ...
In this thesis, synthetic chemistry was used as a tool in the exploration of various aspects of natu...
The cobalt-catalysed oxidative cyclisation of 5-hydroxy alkenes has been demonstrated to be a powerf...
This thesis describes the development of methods and strategies inspired by three natural products: ...
Three aspects of the protecting-group-free (PGF) synthesis of small molecules have been described in...
The first chapter describes our preparation of novel analogs of the natural product, palmarumycin CP...