We report here a simple and robust gold-catalyzed annulation reaction, giving N- and O-spirocycles in good to excellent yields. We have prepared a library of protected amines and tertiary alcohols that give, upon cyclization with alkynes, a representative set of heterospirocycles and illustrate reaction compatibility with diverse functional groups. A change in catalytic activity is possible by modifying the solvent, and two original tricyclic spirocycles were synthesized in a tandem reaction.Synthèse Organique : des molécules au vivantRadiopharmaceutiques Innovants en Oncologie et Neurologi
The work in this thesis was undertaken in Chemistry and Biological Chemistry, School of Physical and...
A versatile approach to the valorization of propargylic alcohols is reported, enabling controlled ac...
A highly efficient synthesis of oxygenated 5,5-spiroketals was performed towards the synthesis of th...
International audienceWe report here a simple and robust gold-catalyzed annulation reaction, giving ...
International audienceGold-(I) catalysis was used for the intramolecular cyclization of tertiary alc...
The work done in the present doctoral thesis, developed in the GlaxoSmithKline Medicine Research Cen...
The first gold(III)-oxazoline catalysed intramolecular tandem dihydroalkoxylations of alkynyl diols ...
This thesis will focus on the development of new methodologies utilizing propargylic alcohols and ac...
We report the use of cationic gold complexes [Au(NHC)(CH<sub>3</sub>CN)][BF<sub>4</sub>] and [{Au...
A highly efficient, gold-catalyzed intramolecular dearomatization reaction of naphthols via 5-endo-d...
International audienceA series of alkynyl ethers react with an electrophilic gold(I) catalyst to pro...
We report the use of cationic gold complexes [Au(NHC)(CH3CN)][BF4] and [{Au(NHC)}(2)(mu-OH)][BF4] (N...
The gold(I)-catalyzed ring-expanding spiroannulation of cyclopropenones with enynes is reported her...
The work in this thesis was undertaken in Chemistry and Biological Chemistry, School of Physical and...
A versatile approach to the valorization of propargylic alcohols is reported, enabling controlled ac...
A highly efficient synthesis of oxygenated 5,5-spiroketals was performed towards the synthesis of th...
International audienceWe report here a simple and robust gold-catalyzed annulation reaction, giving ...
International audienceGold-(I) catalysis was used for the intramolecular cyclization of tertiary alc...
The work done in the present doctoral thesis, developed in the GlaxoSmithKline Medicine Research Cen...
The first gold(III)-oxazoline catalysed intramolecular tandem dihydroalkoxylations of alkynyl diols ...
This thesis will focus on the development of new methodologies utilizing propargylic alcohols and ac...
We report the use of cationic gold complexes [Au(NHC)(CH<sub>3</sub>CN)][BF<sub>4</sub>] and [{Au...
A highly efficient, gold-catalyzed intramolecular dearomatization reaction of naphthols via 5-endo-d...
International audienceA series of alkynyl ethers react with an electrophilic gold(I) catalyst to pro...
We report the use of cationic gold complexes [Au(NHC)(CH3CN)][BF4] and [{Au(NHC)}(2)(mu-OH)][BF4] (N...
The gold(I)-catalyzed ring-expanding spiroannulation of cyclopropenones with enynes is reported her...
The work in this thesis was undertaken in Chemistry and Biological Chemistry, School of Physical and...
A versatile approach to the valorization of propargylic alcohols is reported, enabling controlled ac...
A highly efficient synthesis of oxygenated 5,5-spiroketals was performed towards the synthesis of th...