International audience2-Oxindoles and 2-coumaranones could be selectively allylated in the presence of low cost catalysts based on nickel, leading selectively to different polysubstituted derivatives. Allyl alcohol was used as an allylating reagent and allowed the synthesis of compounds under neutral conditions with water produced as the sole by-product. Experiments have been performed in batch and in flow chemistry. The latter protocol in flow led to a very efficient and straightforward allylic alkylation of 2-oxindoles in only a few minutes with high chemoselectivities towards either the C,C-bisallylated product or the C,C,N-trisallylated one
Transition-metal-catalyzed cross-coupling reactions are reliable tools for forging C–C bonds. The En...
Allylic moiety, an important structural motif in organic chemistry, can be easily transformed into m...
A highly atom-economical allylation of oxindoles with vinyl cyclopropanes catalyzed by Pd(PPh3)(4) h...
International audienceAn additive-free nickel-catalyzed α-allylation of aldehydes with allyl alcohol...
An additive-free nickel-catalyzed alpha-allylation of aldehydes with allyl alcohol is reported. The ...
A nickel catalyst for the allylboration of aldehydes is reported, facilitating the preparation of ho...
International audienceA clean method has been developed for the α-allylation of phenyl and alpha alk...
Carbonyl-containing oxindoles are ubiquitous core structures present in many biologically active nat...
Nickel hydride type complexes have been successfully developed as catalysts for the tandem isomeriza...
En synthèse organique, les réactions d’allylation utilisant des métaux de transition tel que le pall...
International audienceα-carbonyl homoallylic alcohols have been synthesized in a one-pot reaction fr...
A functional group exchange reaction between allylamines and alkenes via nickel-catalyzed CC bond ...
A "totally catalytic" nickel(0)-mediated method for base-free direct alkylation of allyl alcohols an...
The preparation of allylic amines is traditionally accomplished by reactions of amines with reactive...
Here we report the application of dual nickel/photoredox catalysis to the allylation of aliphatic, a...
Transition-metal-catalyzed cross-coupling reactions are reliable tools for forging C–C bonds. The En...
Allylic moiety, an important structural motif in organic chemistry, can be easily transformed into m...
A highly atom-economical allylation of oxindoles with vinyl cyclopropanes catalyzed by Pd(PPh3)(4) h...
International audienceAn additive-free nickel-catalyzed α-allylation of aldehydes with allyl alcohol...
An additive-free nickel-catalyzed alpha-allylation of aldehydes with allyl alcohol is reported. The ...
A nickel catalyst for the allylboration of aldehydes is reported, facilitating the preparation of ho...
International audienceA clean method has been developed for the α-allylation of phenyl and alpha alk...
Carbonyl-containing oxindoles are ubiquitous core structures present in many biologically active nat...
Nickel hydride type complexes have been successfully developed as catalysts for the tandem isomeriza...
En synthèse organique, les réactions d’allylation utilisant des métaux de transition tel que le pall...
International audienceα-carbonyl homoallylic alcohols have been synthesized in a one-pot reaction fr...
A functional group exchange reaction between allylamines and alkenes via nickel-catalyzed CC bond ...
A "totally catalytic" nickel(0)-mediated method for base-free direct alkylation of allyl alcohols an...
The preparation of allylic amines is traditionally accomplished by reactions of amines with reactive...
Here we report the application of dual nickel/photoredox catalysis to the allylation of aliphatic, a...
Transition-metal-catalyzed cross-coupling reactions are reliable tools for forging C–C bonds. The En...
Allylic moiety, an important structural motif in organic chemistry, can be easily transformed into m...
A highly atom-economical allylation of oxindoles with vinyl cyclopropanes catalyzed by Pd(PPh3)(4) h...