A spirocyclic, sp3-atom rich oxetane-containing scaffold was synthesised in just two steps via a gold catalysed propargylic alcohol rearrangement. The key gold cyclisation can be undertaken on a 40 g scale allowing the preparation of 419 lead-like compounds based on the scaffold for the European Lead Factory
AbstractOwing to their inherent three-dimensionality and structural novelty, spiro scaffolds have be...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
Controlling the properties of lead molecules is critical in drug discovery, but sourcing large numbe...
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...
The synthesis of large numbers of diverse molecular scaffolds with controlled molecular properties i...
Ring-opening of cyclic sulfamidates with propargylic sulfonamides yielded substrates for a gold-cata...
Recently we have documented research efforts aimed at new classes of oxetanes as well as spirohetero...
This report describes the preparation of a series of 17 novel racemic spirocyclic scaffolds that are...
Oxetane-benzopyran spirocycles were synthesised via a palladium catalysed cyclisation-cross coupling...
Spiropiperidines have been labelled as 'privileged structures' in regard to their ability to provide...
In order to address the current downturn in the drug discovery pipeline, initiatives are being under...
A simple two-step sequence is used to efficiently make novel spirocyclic analogues of the diketopipe...
A modular synthetic approach was developed that yielded thirty diverse lead-like scaffolds suitable ...
AbstractOwing to their inherent three-dimensionality and structural novelty, spiro scaffolds have be...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
Controlling the properties of lead molecules is critical in drug discovery, but sourcing large numbe...
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...
The synthesis of large numbers of diverse molecular scaffolds with controlled molecular properties i...
Ring-opening of cyclic sulfamidates with propargylic sulfonamides yielded substrates for a gold-cata...
Recently we have documented research efforts aimed at new classes of oxetanes as well as spirohetero...
This report describes the preparation of a series of 17 novel racemic spirocyclic scaffolds that are...
Oxetane-benzopyran spirocycles were synthesised via a palladium catalysed cyclisation-cross coupling...
Spiropiperidines have been labelled as 'privileged structures' in regard to their ability to provide...
In order to address the current downturn in the drug discovery pipeline, initiatives are being under...
A simple two-step sequence is used to efficiently make novel spirocyclic analogues of the diketopipe...
A modular synthetic approach was developed that yielded thirty diverse lead-like scaffolds suitable ...
AbstractOwing to their inherent three-dimensionality and structural novelty, spiro scaffolds have be...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
Controlling the properties of lead molecules is critical in drug discovery, but sourcing large numbe...