A practical method for the synthesis of phenyl enol ethers is reported. The combination of a gold(I) catalyst and potassium carbonate selectively mediates the addition of phenols to propargylic alcohols/amines in a chemo-, regio-, and stereoselective fashion in high yield. The resulting enol ethers are formed exclusively with a Z-configuration and can be obtained from a wide array of phenols and propargylic alcohols or amines with the reaction showing excellent functional group tolerance
Due to the synthetic advantages presented by the dual-gold-catalysed hydrophenoxylation of alkynes, ...
Au(I) catalysis has recently emerged as a powerful tool for the realization of a broad range of orga...
The compatibility between gold(I) catalysts and amine transaminases has been explored to transform r...
A practical method for the synthesis of phenyl enol ethers is reported. The combination of a gold(I)...
A versatile approach to the valorization of propargylic alcohols is reported, enabling controlled ac...
Propargylic alcohols are easily accessed through the reaction of alkynes with aldehydes and ketones....
The regioselective gold-catalysed hydration of propargylic alcohols to β-hydroxy ketones can be achi...
A versatile approach to the valorization of propargylic alcohols is reported, enabling controlled ac...
The EPSRC and ERC are gratefully acknowledged for support.We report the use of cationic gold complex...
This thesis will focus on the development of new methodologies utilizing propargylic alcohols and ac...
Inductive perturbations of C-C triple bonds are shown to dictate the regiochemistry of gold-catalyze...
Using the previously designed biphenyl-2-ylphosphine ligand, featuring a remote tertiary amino group...
This article belongs to the Special Issue Catalytic Approaches to Selective Elaboration of Organic M...
ABSTRACT FOR PART I: HYDROPHENOXYLATION REACTIONS CATALYZED BY ARYLGOLD(I) COMPOUNDS Both carbine an...
The EPSRC and ERC are gratefully acknowledged for support. S.P.N. is a Royal Society Wolfson Researc...
Due to the synthetic advantages presented by the dual-gold-catalysed hydrophenoxylation of alkynes, ...
Au(I) catalysis has recently emerged as a powerful tool for the realization of a broad range of orga...
The compatibility between gold(I) catalysts and amine transaminases has been explored to transform r...
A practical method for the synthesis of phenyl enol ethers is reported. The combination of a gold(I)...
A versatile approach to the valorization of propargylic alcohols is reported, enabling controlled ac...
Propargylic alcohols are easily accessed through the reaction of alkynes with aldehydes and ketones....
The regioselective gold-catalysed hydration of propargylic alcohols to β-hydroxy ketones can be achi...
A versatile approach to the valorization of propargylic alcohols is reported, enabling controlled ac...
The EPSRC and ERC are gratefully acknowledged for support.We report the use of cationic gold complex...
This thesis will focus on the development of new methodologies utilizing propargylic alcohols and ac...
Inductive perturbations of C-C triple bonds are shown to dictate the regiochemistry of gold-catalyze...
Using the previously designed biphenyl-2-ylphosphine ligand, featuring a remote tertiary amino group...
This article belongs to the Special Issue Catalytic Approaches to Selective Elaboration of Organic M...
ABSTRACT FOR PART I: HYDROPHENOXYLATION REACTIONS CATALYZED BY ARYLGOLD(I) COMPOUNDS Both carbine an...
The EPSRC and ERC are gratefully acknowledged for support. S.P.N. is a Royal Society Wolfson Researc...
Due to the synthetic advantages presented by the dual-gold-catalysed hydrophenoxylation of alkynes, ...
Au(I) catalysis has recently emerged as a powerful tool for the realization of a broad range of orga...
The compatibility between gold(I) catalysts and amine transaminases has been explored to transform r...