An improved protocol for the Meyer- Schuster rearrangement with dinuclear gold complexes allowing for low catalyst loadings is presented. The new protocol has been successfully applied to the synthesis of prostaglandins. This study helps exclude earlier mechanistic proposals and highlights the relevance and possibly more significant role of digold complexes in gold catalysis
Readily available phosphoramidites incorporating TADDOL-related diols with an acyclic backbone turne...
Propargylic alcohols are easily accessed through the reaction of alkynes with aldehydes and ketones....
Over the years, gold catalysis has materialized as an incredible synthetic approach among the scient...
An improved protocol for the Meyer- Schuster rearrangement with dinuclear gold complexes allowing fo...
Gold(I) mediated Meyer Schuster rearrangement for the installation of the 'lower' side chain of pros...
With the aim of rationalizing the experimental counterion- and solvent-dependent reactivity in the g...
Under dual gold/photoredox catalytic conditions, intermediates from the Meyer-Schuster rearrangement...
Gold(I) mediated MeyereSchuster rearrangement for the installation of the ‘lower’ side chain of pros...
communicationInternational audienceA study concerning the gold(I) catalyzed rearrangement of proparg...
Novel organic reactions drive the advance of chemical synthesis in the same way that enabling techno...
The gold/silver-cocatalyzed conversion of aldoximes into primary amides is reported. The reaction, w...
In this dissertation, gold catalyst was employed to catalyze intermolecular reactions. Intramolecula...
In the past dozen years, great progress has been made in developing highly efficient homogenous gold...
The gold/silver-cocatalyzed conversion of aldoximes into primary amides is reported. The reaction, w...
International audienceDiversely substituted 4-alkylidene-1,3-dioxolan-2-ones are efficiently synthes...
Readily available phosphoramidites incorporating TADDOL-related diols with an acyclic backbone turne...
Propargylic alcohols are easily accessed through the reaction of alkynes with aldehydes and ketones....
Over the years, gold catalysis has materialized as an incredible synthetic approach among the scient...
An improved protocol for the Meyer- Schuster rearrangement with dinuclear gold complexes allowing fo...
Gold(I) mediated Meyer Schuster rearrangement for the installation of the 'lower' side chain of pros...
With the aim of rationalizing the experimental counterion- and solvent-dependent reactivity in the g...
Under dual gold/photoredox catalytic conditions, intermediates from the Meyer-Schuster rearrangement...
Gold(I) mediated MeyereSchuster rearrangement for the installation of the ‘lower’ side chain of pros...
communicationInternational audienceA study concerning the gold(I) catalyzed rearrangement of proparg...
Novel organic reactions drive the advance of chemical synthesis in the same way that enabling techno...
The gold/silver-cocatalyzed conversion of aldoximes into primary amides is reported. The reaction, w...
In this dissertation, gold catalyst was employed to catalyze intermolecular reactions. Intramolecula...
In the past dozen years, great progress has been made in developing highly efficient homogenous gold...
The gold/silver-cocatalyzed conversion of aldoximes into primary amides is reported. The reaction, w...
International audienceDiversely substituted 4-alkylidene-1,3-dioxolan-2-ones are efficiently synthes...
Readily available phosphoramidites incorporating TADDOL-related diols with an acyclic backbone turne...
Propargylic alcohols are easily accessed through the reaction of alkynes with aldehydes and ketones....
Over the years, gold catalysis has materialized as an incredible synthetic approach among the scient...