We demonstrate that a diboration‐electrocyclization sequence provides access to a range of pyridine fused small molecule boronic ester building blocks, and that these are amenable to high throughput synthesis leading to biaryl and ether linked compound libraries. Moreover, the implementation of an integrated physchem and ADME profiling workflow allows accelerated design of novel lead compounds for application in drug discovery projects
The confidentiality statement on each page of this thesis DOES NOT apply.Previously held under morat...
Complementary cyclisation reactions of hex-2-ene-1,6-diamine derivatives were exploited in the synth...
The greater geometric lability of hydrazones compared to that of oxime ethers is used as a basis to ...
A new and efficient synthesis of pyridine‐based heteroaromatic boronic acid derivatives is reported ...
A new and efficient synthesis of pyridine-based heteroaromatic boronic acid derivatives is reported ...
Current approaches to drug discovery tends to involve the rapid analogue synthesis and testing of sm...
A continuous flow process delivering key building blocks for a series of BCP modulator libraries is ...
Synthesising polar semi-saturated bicyclic heterocycles can lead to better starting points for fragm...
Chemically generated libraries of small, non-oligomeric compounds are being widely embraced by resea...
The availability of suitable diverse fragment- and lead-oriented screening compounds is key for the ...
A multi-gram-scale synthetic route to a novel, bifunctional normorphan 3D building block bearing ort...
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tri...
Small molecule libraries have become essential for the development of drug discovery campaigns and ...
An innovative and efficient reagent- and scaffold-based diversity oriented synthesis (DOS) of a frag...
We report a novel and general method to access a highly under‐studied privileged scaffold – pyrimidi...
The confidentiality statement on each page of this thesis DOES NOT apply.Previously held under morat...
Complementary cyclisation reactions of hex-2-ene-1,6-diamine derivatives were exploited in the synth...
The greater geometric lability of hydrazones compared to that of oxime ethers is used as a basis to ...
A new and efficient synthesis of pyridine‐based heteroaromatic boronic acid derivatives is reported ...
A new and efficient synthesis of pyridine-based heteroaromatic boronic acid derivatives is reported ...
Current approaches to drug discovery tends to involve the rapid analogue synthesis and testing of sm...
A continuous flow process delivering key building blocks for a series of BCP modulator libraries is ...
Synthesising polar semi-saturated bicyclic heterocycles can lead to better starting points for fragm...
Chemically generated libraries of small, non-oligomeric compounds are being widely embraced by resea...
The availability of suitable diverse fragment- and lead-oriented screening compounds is key for the ...
A multi-gram-scale synthetic route to a novel, bifunctional normorphan 3D building block bearing ort...
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tri...
Small molecule libraries have become essential for the development of drug discovery campaigns and ...
An innovative and efficient reagent- and scaffold-based diversity oriented synthesis (DOS) of a frag...
We report a novel and general method to access a highly under‐studied privileged scaffold – pyrimidi...
The confidentiality statement on each page of this thesis DOES NOT apply.Previously held under morat...
Complementary cyclisation reactions of hex-2-ene-1,6-diamine derivatives were exploited in the synth...
The greater geometric lability of hydrazones compared to that of oxime ethers is used as a basis to ...