A new visible-light photocatalytic multicomponent reaction (MCR) involving N-alkyl-N-methylanilines, N-isocyanoiminotriphenylphosphorane, and carboxylic acids leading to 1,3,4-oxadiazole derivatives is reported. The developed mild reaction conditions enable a broad substrate scope and good functional group tolerance, as further highlighted in the late-stage functionalization of amino acids and drugs. Additionally, a two-step one-pot protocol for the synthesis of non-symmetrical diacylhydrazines is also reported
International audienceWe report the synthesis of various phthalazines via a new cascade reaction, in...
Visible light catalysis assisted site-specific modification of α-amino acids by C–H bond functionali...
Novel scaffolds are of uttermost importance for the discovery of functional material. Three differen...
A new visible-light photocatalytic multicomponent reaction (MCR) involving N-alkyl-N-methylanilines,...
The possibility of harnessing the photoactivity of isocyanides in the development of metal-free Ugi-...
A general synthesis of N-protected primary α-amino 1,3,4-oxadiazoles, from N-carbamoyl imines, N-iso...
A new visible light-induced photocatalytic protocol enabling the formation of secondary amides from ...
A new visible light-induced photocatalytic protocol enabling the formation of secondary amides from ...
Oxidative three-component reactions for the direct synthesis of α-amino amides and imides from terti...
With the endeavor to find new efficient synthetic methods to rapidly access diverse molecular struct...
A novel [3 + 2] cycloaddition/oxidative aromatization sequence via visible light-induced photoredox ...
Visible light catalysis allows the regioselective synthesis of oxazolines in high yields. The mild p...
Azetidines are four-membered nitrogen-containing heterocycles that hold great promise in current med...
Substituted imidazoles are traditionally synthesized by co-condensation of multiple feedstocks. Here...
Reported is the controllable selectivity syntheses of four distinct products from the same starting ...
International audienceWe report the synthesis of various phthalazines via a new cascade reaction, in...
Visible light catalysis assisted site-specific modification of α-amino acids by C–H bond functionali...
Novel scaffolds are of uttermost importance for the discovery of functional material. Three differen...
A new visible-light photocatalytic multicomponent reaction (MCR) involving N-alkyl-N-methylanilines,...
The possibility of harnessing the photoactivity of isocyanides in the development of metal-free Ugi-...
A general synthesis of N-protected primary α-amino 1,3,4-oxadiazoles, from N-carbamoyl imines, N-iso...
A new visible light-induced photocatalytic protocol enabling the formation of secondary amides from ...
A new visible light-induced photocatalytic protocol enabling the formation of secondary amides from ...
Oxidative three-component reactions for the direct synthesis of α-amino amides and imides from terti...
With the endeavor to find new efficient synthetic methods to rapidly access diverse molecular struct...
A novel [3 + 2] cycloaddition/oxidative aromatization sequence via visible light-induced photoredox ...
Visible light catalysis allows the regioselective synthesis of oxazolines in high yields. The mild p...
Azetidines are four-membered nitrogen-containing heterocycles that hold great promise in current med...
Substituted imidazoles are traditionally synthesized by co-condensation of multiple feedstocks. Here...
Reported is the controllable selectivity syntheses of four distinct products from the same starting ...
International audienceWe report the synthesis of various phthalazines via a new cascade reaction, in...
Visible light catalysis assisted site-specific modification of α-amino acids by C–H bond functionali...
Novel scaffolds are of uttermost importance for the discovery of functional material. Three differen...