In order to address the current downturn in the drug discovery pipeline, initiatives are being undertaken to synthesise screening libraries of sp3-rich, low molecular weight compounds. As part of the European Lead Factory initiative, the synthesis and derivatisation of a simple hexahydrooxazolo[5,4-c]pyridin-2(1H)-one bicyclic carbamate has been achieved. The synthetic route employed involved a telescoped hetero-Diels–Alder/[2,3]-sigmatropic rearrangement/cyclisation sequence to deliver the desired core scaffold containing two points for further diversification. When applied, this synthesis was found to be robust and scalable which allowed the production of a 155 compound library
The screening of compound libraries has repeatedly demonstrated its effectiveness as a research tool...
We demonstrate that a diboration‐electrocyclization sequence provides access to a range of pyridine ...
The utilization of Baylis-Hillman and oxa-Michael methodologies for the synthesis of sultam (cyclic ...
In order to address the current downturn in the drug discovery pipeline, initiatives are being under...
The reaction conditions for an enantiospecific synthesis of various N-aryl-oxazolidinones from N-ary...
5‐Oxazoyl‐sulfamates have been profiled as versatile building blocks for modifications of oxazoles w...
The preparation of sp3-rich scaffolds to obtain more natural product-like libraries for incorporatio...
AbstractAn efficient synthetic access to two amino-oxazoline compound libraries was developed employ...
Synthesising polar semi-saturated bicyclic heterocycles can lead to better starting points for fragm...
A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is ba...
A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is ba...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
We have successfully implemented the concept of Distributed Drug Discovery (D3) in the search for CN...
The screening of compound libraries has repeatedly demonstrated its effectiveness as a research tool...
We demonstrate that a diboration‐electrocyclization sequence provides access to a range of pyridine ...
The utilization of Baylis-Hillman and oxa-Michael methodologies for the synthesis of sultam (cyclic ...
In order to address the current downturn in the drug discovery pipeline, initiatives are being under...
The reaction conditions for an enantiospecific synthesis of various N-aryl-oxazolidinones from N-ary...
5‐Oxazoyl‐sulfamates have been profiled as versatile building blocks for modifications of oxazoles w...
The preparation of sp3-rich scaffolds to obtain more natural product-like libraries for incorporatio...
AbstractAn efficient synthetic access to two amino-oxazoline compound libraries was developed employ...
Synthesising polar semi-saturated bicyclic heterocycles can lead to better starting points for fragm...
A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is ba...
A new route to spiro-oxetanes, potential scaffolds for drug discovery, is described. The route is ba...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
We have successfully implemented the concept of Distributed Drug Discovery (D3) in the search for CN...
The screening of compound libraries has repeatedly demonstrated its effectiveness as a research tool...
We demonstrate that a diboration‐electrocyclization sequence provides access to a range of pyridine ...
The utilization of Baylis-Hillman and oxa-Michael methodologies for the synthesis of sultam (cyclic ...