Authors acknowledge The University of St Andrews (JB) and the EaSICAT Centre for Doctoral Training (MTW) for funding.α,β-Unsaturated acyl ammonium species are versatile intermediates that have been applied in a variety of transformations including Michael additions, domino reactions and cycloadditions. Many of these transformations are promoted by chiral Lewis base catalysts, enabling the rapid generation of molecular complexity with high stereochemical control. This review highlights recent developments in the generation and application of α,β-unsaturated acyl ammonium intermediates reported since a previous review of this area in 2016. Particular emphasis will be placed on reports providing mechanistic insight into catalytic transformatio...
The developments of novel catalytic transformations are just as important as the discoveries of new ...
The authors thank the European Research Council under the European Union’s Seventh Framework Program...
This tutorial review highlights the organocatalytic Lewis base functionalisation of carboxylic acids...
α,β-Unsaturated acyl ammonium species are versatile intermediates that have been applied in a variet...
This thesis details investigations into the generation and synthetic utility of α,β-unsaturated acyl...
The research described in this thesis focuses on probing the reactivity of α,β-unsaturated acyl ammo...
The authors thank the European Research Council under the European Union's Seventh Framework Program...
The asymmetric annulation of a range of alpha,beta-unsaturated acyl ammonium intermediates, formed f...
The asymmetric annulation of a range of alpha,beta-unsaturated acyl ammonium intermediates, formed f...
We thank the European Research Council under the European Union’s Seventh Framework Programme (FP7/2...
We thank the European Research Council under the European Union’s Seventh Framework Programme (FP7/2...
Funding: UK EPSRC (EP/M508214/1, C.M.). Royal Society for a Wolfson Research Merit Award (A.D.S.).C(...
The authors thank Syngenta and the EPSRC Centre for Doctoral Training in Critical Resource Catalysis...
© 2018 The Royal Society of Chemistry. An isothiourea-catalysed Michael addition-annulation process ...
The developments of novel catalytic transformations are just as important as the discoveries of new ...
The developments of novel catalytic transformations are just as important as the discoveries of new ...
The authors thank the European Research Council under the European Union’s Seventh Framework Program...
This tutorial review highlights the organocatalytic Lewis base functionalisation of carboxylic acids...
α,β-Unsaturated acyl ammonium species are versatile intermediates that have been applied in a variet...
This thesis details investigations into the generation and synthetic utility of α,β-unsaturated acyl...
The research described in this thesis focuses on probing the reactivity of α,β-unsaturated acyl ammo...
The authors thank the European Research Council under the European Union's Seventh Framework Program...
The asymmetric annulation of a range of alpha,beta-unsaturated acyl ammonium intermediates, formed f...
The asymmetric annulation of a range of alpha,beta-unsaturated acyl ammonium intermediates, formed f...
We thank the European Research Council under the European Union’s Seventh Framework Programme (FP7/2...
We thank the European Research Council under the European Union’s Seventh Framework Programme (FP7/2...
Funding: UK EPSRC (EP/M508214/1, C.M.). Royal Society for a Wolfson Research Merit Award (A.D.S.).C(...
The authors thank Syngenta and the EPSRC Centre for Doctoral Training in Critical Resource Catalysis...
© 2018 The Royal Society of Chemistry. An isothiourea-catalysed Michael addition-annulation process ...
The developments of novel catalytic transformations are just as important as the discoveries of new ...
The developments of novel catalytic transformations are just as important as the discoveries of new ...
The authors thank the European Research Council under the European Union’s Seventh Framework Program...
This tutorial review highlights the organocatalytic Lewis base functionalisation of carboxylic acids...