We report direct activation of allylic alcohols using a hydrogen-bond-assisted palladium catalyst and use this for alkylation and amination reactions. The novel catalyst comprises a palladium complex based on a functionalized monodentate phosphoramidite ligand in combination with urea additives and affords linear alkylated and aminated allylic products selectively. Detailed kinetic analysis show that oxidative addition of the allyl alcohol is the rate-determining step, which is facilitated by hydrogen bonds between the alcohol, the ligand functional group, and the additional urea additive
A new class of palladium complexes bearing bidentate 2-hydroxypyridine based ligands have been prepa...
Using modular, monodentate phosphoramidite ligands, enantioselective palladium catalysed diethylzinc...
This thesis is based on the development of novel catalytic reactions for the synthesis and applicati...
We here report a computational approach on the mechanism of allylicamination reactions using allyl-a...
The direct use of allylic alcohols in substitution reactions without pre-activation of the hydroxyl-...
The direct dehydrative activation of allylic alcohols and subsequent cross-coupling with alkenes by ...
The direct electrophilic, nucleophilic, and amphiphilic allylations of allylic alcohol by use of a p...
In-situ activation of a variety of allylic alcohols by hexachlorophosphazene (or oxalyl chloride) fo...
This thesis deals with the palladium-catalyzed nucleophilic substitution of π-activated alcohols in ...
Palladium complexes supported by tridentate phosphido diphosphine ligands (P(o-C6H4PR2)2: 1, R = iPr...
The combination of Pd catalyst and triethylborane induces allylic alcohols to undergo direct electro...
A mild and efficient dehydrative cross-coupling reaction between allylic alcohols and N-heterocycles...
The selective formation of new carbon-carbon bonds is a central challenge for organic synthesis; org...
The selective palladium-catalyzed carboamination of allylic alcohols is reported on the basis of the...
International audienceA cationic xanthene phosphole palladium allyl complex efficiently catalyzes th...
A new class of palladium complexes bearing bidentate 2-hydroxypyridine based ligands have been prepa...
Using modular, monodentate phosphoramidite ligands, enantioselective palladium catalysed diethylzinc...
This thesis is based on the development of novel catalytic reactions for the synthesis and applicati...
We here report a computational approach on the mechanism of allylicamination reactions using allyl-a...
The direct use of allylic alcohols in substitution reactions without pre-activation of the hydroxyl-...
The direct dehydrative activation of allylic alcohols and subsequent cross-coupling with alkenes by ...
The direct electrophilic, nucleophilic, and amphiphilic allylations of allylic alcohol by use of a p...
In-situ activation of a variety of allylic alcohols by hexachlorophosphazene (or oxalyl chloride) fo...
This thesis deals with the palladium-catalyzed nucleophilic substitution of π-activated alcohols in ...
Palladium complexes supported by tridentate phosphido diphosphine ligands (P(o-C6H4PR2)2: 1, R = iPr...
The combination of Pd catalyst and triethylborane induces allylic alcohols to undergo direct electro...
A mild and efficient dehydrative cross-coupling reaction between allylic alcohols and N-heterocycles...
The selective formation of new carbon-carbon bonds is a central challenge for organic synthesis; org...
The selective palladium-catalyzed carboamination of allylic alcohols is reported on the basis of the...
International audienceA cationic xanthene phosphole palladium allyl complex efficiently catalyzes th...
A new class of palladium complexes bearing bidentate 2-hydroxypyridine based ligands have been prepa...
Using modular, monodentate phosphoramidite ligands, enantioselective palladium catalysed diethylzinc...
This thesis is based on the development of novel catalytic reactions for the synthesis and applicati...