An efficient synthetic route towards tosyl-protected (2S)-phenyl-3-piperidone, a common intermediate for many drugs, has been developed in 5 steps in 54% yield from biomass derived furfural. The synthetic utility of the piperidone core structure was demonstrated with the synthesis of a NK1 receptor antagonist.Published versio
The total synthesis of natural products and their analogs is a very exciting and challenging area of...
Single isomers of the furanylidene system 8 were synthesized in four steps. The synthesis begins wit...
Natural products have until recently provided the only remedy for treatment of diseases. The develop...
This thesis details the design, development and execution of innovative methodology in the total syn...
In this thesis, the conversion of biomass to several high value chemicals via versatile and syntheti...
The antifungal activity of α, β-unsaturated carbonyl compounds has been recognized generally due to ...
Reductive amination of 2,5-diformylfuran (DFF) was used to implement the transition from bio-derived...
Synthesis of NK-1 antagonists Lucie Puchnerová Department of Organic and Pharmaceutical Chemistry, F...
This report describes the preparation of a series of 17 novel racemic spirocyclic scaffolds that are...
The preparation of medicinally relevant small molecules from biomass is a field of interest due to: ...
Furanokurzin is a recently discovered compound that was found to inhibit acetylcholinesterase enzyme...
A concise (5 to 6 steps), stereodivergent, highly diastereoselective (dr up to >19:1 for both stereo...
The tachykinins are a family of neuropeptides found in the body that have been implicated in a varie...
The [4+2] cycloaddition leads to rapid formation of molecular complexity that can be achieved in a s...
Polyalkyl furans are widespread in nature, often performing important biological roles. Despite a pl...
The total synthesis of natural products and their analogs is a very exciting and challenging area of...
Single isomers of the furanylidene system 8 were synthesized in four steps. The synthesis begins wit...
Natural products have until recently provided the only remedy for treatment of diseases. The develop...
This thesis details the design, development and execution of innovative methodology in the total syn...
In this thesis, the conversion of biomass to several high value chemicals via versatile and syntheti...
The antifungal activity of α, β-unsaturated carbonyl compounds has been recognized generally due to ...
Reductive amination of 2,5-diformylfuran (DFF) was used to implement the transition from bio-derived...
Synthesis of NK-1 antagonists Lucie Puchnerová Department of Organic and Pharmaceutical Chemistry, F...
This report describes the preparation of a series of 17 novel racemic spirocyclic scaffolds that are...
The preparation of medicinally relevant small molecules from biomass is a field of interest due to: ...
Furanokurzin is a recently discovered compound that was found to inhibit acetylcholinesterase enzyme...
A concise (5 to 6 steps), stereodivergent, highly diastereoselective (dr up to >19:1 for both stereo...
The tachykinins are a family of neuropeptides found in the body that have been implicated in a varie...
The [4+2] cycloaddition leads to rapid formation of molecular complexity that can be achieved in a s...
Polyalkyl furans are widespread in nature, often performing important biological roles. Despite a pl...
The total synthesis of natural products and their analogs is a very exciting and challenging area of...
Single isomers of the furanylidene system 8 were synthesized in four steps. The synthesis begins wit...
Natural products have until recently provided the only remedy for treatment of diseases. The develop...