The dissertation aimed at the development of a synthetic strategy towards the polyketide Enterocin, using a meta-photocycloaddition as the key step. In the course of methodological studies, an interesting correlation between the installed benzylic substituent and the obtained regioisomeric ratio of photoproducts was discovered. Furthermore, novel methods for the functionalization of photoproducts were explored. However, the planned strategy could not be realized and the construction of the core structure was therefore examined with aldol reactions as pivotal transformations.
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The dissertation aimed at the development of a synthetic strategy towards the polyketide Enterocin, using a meta-photocycloaddition as the key step. In the course of methodological studies, an interesting correlation between the installed benzylic substituent and the obtained regioisomeric ratio of photoproducts was discovered. Furthermore, novel methods for the functionalization of photoproducts were explored. However, the planned strategy could not be realized and the construction of the core...
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