Towards the Asymmetric Synthesis of 1,2-Oxazines
The present work dealt with the preparation of some key intermediates and their use for the generation of chemical diversity.
In Chapter 2 the synthesis of cycloadducts 2.24 was attempted starting fiom acyl nitroso species 2.2.
In Chapter 3 a novel route to alkene-functionalised monobactams was developed and their potential in diversity oriented synthesis is still in progress.
In Chapter 4 we have described a good enantioselective Michael-initiated ring closure (MIRC) reaction of 2,3 -substituted- 1,1 -cyclopropanediesters under operationally simple conditions and mild PTC catalysis. The study delivers a class of novel enantiopure Michael adducts which could serve as valuable building blocks and as templates of high potential synthetic utility.
History
First Supervisor
Dr Mauro AdamoSecond Supervisor
Dr Francesco FiniComments
A thesis submitted to the Royal College of Surgeons in Ireland for the degree of Doctor of Philosophy from the National University of Ireland in 2010.Published Citation
Piras L. Towards the Asymmetric Synthesis of 1,2-Oxazines [PhD Thesis]. Dublin: Royal College of Surgeons in Ireland; 2010Degree Name
- Doctor of Philosophy (PhD)
Date of award
2010-06-30Usage metrics
