Reference: Maria Gerelle, (2012). Synthesis and elaboration of heterocycles via palladium-catalyzed C-H functionalization. DPhil. University of Oxford.Citable link to this page:
Chapter 1 is a brief literature review of the most recent progress in the area of C-H functionalization via palladium catalysis. This covers the functionalization of electron deficient arenes and heterocycles with alkenyl and alkyl halides both using inter- and intra-molecular reactions. The chapter also contains an overview of recent work from the Willis group.
Chapter 2 presents the functionalization of electron deficient arenes and alkenyl bromides using palladium catalysis, as well as the use of statistical analysis software for optimizing the cross-coupling reaction.
Chapter 3 describes the cross-coupling of substituted benzoxazoles, benzothiazole and benzimidazole with a range of alkenyl iodides using palladium catalysis. The reaction can tolerate both (E) and (Z) disubstituted alkenes and tri-substituted alkenyl iodides, with retention of the double bond geometry.
Chapter 4 details the synthesis of sultams via an intramolecular C-H functionalization using palladium catalysis. The chapter covers the optimization of the starting material synthesis as well as the cross-coupling reaction. We can access the sulfonamides from cyclohexenone and were able to incorporate a large range of substitution patterns (Scheme 3).
Finally, Chapter 5 contains all the experimental details, general considerations and compound data. All the NMR spectra of novel compounds can be found in the appendix.
|Digital Origin:||Born digital|
|Type of Award:||DPhil|
|Level of Award:||Doctoral|
|Awarding Institution:||University of Oxford|
|Notes:||This thesis is not currently available via ORA.|
|Copyright Holder:||Maria Gerelle|
|Access Condition:||Restricted: Full content available from 2015-09-28 (ISO 8601)|