Search results for "Heterocyclic chemistry"
showing 5 items of 5 documents
Synthesis, Reactivity, Biological Activity and Applications of Fluorinated Oxadiazoles and Thiadiazoles
2014
A literature survey of the chemistry of fluorinated oxadiazoles and thiadiazoles is presented. The core part on synthetic procedures is given by type of heterocycle and includes recent developments up to the end of 2012. Reactivity is discussed when induced by the presence of the fluorinated moiety. Selected examples of bioactive compounds and applications are illustrated.
Electrochemical synthesis of carbazoles by dehydrogenative coupling reaction
2020
Abstract A constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N‐protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.
Polifunkcionālo kvaternizēto piridina atvasinājumu sintēze un īpašības
2003
Advisor: Duburs, Gunārs ; Tirzītis, Gunārs
SYNTHESIS OF HETEROCYCLES IN NON-CONVENTIONAL MEDIA: THE CASE OF IONIC LIQUIDS
2022
The synthesis of heterocycles is a prominent feature of organic chemistry, due to the enormous importance of such compounds in fields like medicinal or industrial chemistry. In the effort of improving their synthesis, the nature of the solvent plays a pivotal role. In this context, the use on non-conventional solvent like ionic liquids can determine significant improvements reaction outcomes, sustainability of the process, and possibility to be coupled with non-conventional synthetic methodologies, like ultrasounds or microwave irradiation. In this chapter, we present a bird’s-eye view on recent examples of the application of ionic liquids as solvents or catalysts, evidencing, whenever poss…
PI-Extension of porphyrins via intramolecular aromatic oxidative C-N coupling
2019
Π-extension of porphyrins has been performed via intramolecular oxidative C-N coupling of peripheral pyridinyl fragment(s) with the porphyrin core. These fusion reactions lead to the formation of C-N bond(s) between the substituent(s) and the porphyrin. The precursors were functionnalized with 2-mercaptopyridine, 8-hydoxyquinoline and 2-picoline at their meso or β-pyrrolic positions via aromatic nucleophlic substitution, cross-coupling reaction or reaction of the macrocycle with organolithium reagents. Voltametric analyses revealed some marked differences on the reactivity of the porphyrins depending on their substitution pattern and metalation (nickel(II) or zinc(II)). Chemical and electro…