A new protocol for the alkylation of aromatic amines has been described using alcohols in the presence of SmI2 as a catalyst with the generation of water as the sole byproduct. The reaction proceeds under MW conditions and selectively generates monoalkylated amines. This protocol features a broad substrate scope and good functional-group tolerance with moderate to high yields
A nonmetal catalyst [Ph<sub>3</sub>C][B(C<sub>6</sub>F<sub>5</sub>)<sub>4</sub>] has been develope...
The N-alkylation of amines with alcohols using earth-abundant and nonprecious metal catalysts has ga...
Department of Chemistry, Faculty of Science, M. L. Sukhadia University, Udaipur-313 002, India E-ma...
Traditionally, anilines can be alkylated with reactive alkyl halides but now more safe reagents such...
International audienceBorrowing hydrogen (or hydrogen autotransfer) reactions represent straightforw...
N-Alkylation reaction of amine functionalized phenylene moieties in crystal-like mesoporous silica i...
Abstract—A new effective catalytic system consisting of [Cp*IrCl2]2/K2CO3 (Cp*=pentamethylcyclopenta...
A new Pd-substituted octahedral molecular sieve (Pd/K-OMS-2) catalyst has been prepared for the dire...
The Zincke reaction allows the transformation of primary amines into their respective <i>N</i>-alkyl...
A method for selective mono-N-alkylation of primary amines to produce secondary amines that are subs...
A base-catalyzed/promoted transition-metal-free direct alkylation of amines with alcohols has been d...
An efficient entry to aromatic amides using microwave irradiation in aqueous medium is described. St...
A new, robust, and reliable method has been developed for the selective reductive N-alkylation of pr...
Highly chemoselective direct reduction of primary, secondary, and tertiary amides to alcohols using ...
A readily available pincer ruthenium(II) complex catalyzes the selective monoalkylation of (hetero)a...
A nonmetal catalyst [Ph<sub>3</sub>C][B(C<sub>6</sub>F<sub>5</sub>)<sub>4</sub>] has been develope...
The N-alkylation of amines with alcohols using earth-abundant and nonprecious metal catalysts has ga...
Department of Chemistry, Faculty of Science, M. L. Sukhadia University, Udaipur-313 002, India E-ma...
Traditionally, anilines can be alkylated with reactive alkyl halides but now more safe reagents such...
International audienceBorrowing hydrogen (or hydrogen autotransfer) reactions represent straightforw...
N-Alkylation reaction of amine functionalized phenylene moieties in crystal-like mesoporous silica i...
Abstract—A new effective catalytic system consisting of [Cp*IrCl2]2/K2CO3 (Cp*=pentamethylcyclopenta...
A new Pd-substituted octahedral molecular sieve (Pd/K-OMS-2) catalyst has been prepared for the dire...
The Zincke reaction allows the transformation of primary amines into their respective <i>N</i>-alkyl...
A method for selective mono-N-alkylation of primary amines to produce secondary amines that are subs...
A base-catalyzed/promoted transition-metal-free direct alkylation of amines with alcohols has been d...
An efficient entry to aromatic amides using microwave irradiation in aqueous medium is described. St...
A new, robust, and reliable method has been developed for the selective reductive N-alkylation of pr...
Highly chemoselective direct reduction of primary, secondary, and tertiary amides to alcohols using ...
A readily available pincer ruthenium(II) complex catalyzes the selective monoalkylation of (hetero)a...
A nonmetal catalyst [Ph<sub>3</sub>C][B(C<sub>6</sub>F<sub>5</sub>)<sub>4</sub>] has been develope...
The N-alkylation of amines with alcohols using earth-abundant and nonprecious metal catalysts has ga...
Department of Chemistry, Faculty of Science, M. L. Sukhadia University, Udaipur-313 002, India E-ma...