A simple and efficient catalytic method for the synthesis of alkenyl halides via direct coupling of alcohols and alkynes using aqueous HX (X=Cl, Br) as halide sources has been developed under mild conditions in the presence of Fe powder (1 mol %). In comparison with the high loading of FeX3 in previously reported protocols, the present approach provides a remarkable attractive methodology to a diverse range of alkenyl halides due to the advantages of simple operation and low-level metal contamination. (C) 2015 Elsevier Ltd. All rights reserved
Cheap, readily available, air stable, nontoxic, and environmentally benign iron salts such as Fe(aca...
While attractive, the iron-catalyzed coupling of arylboron reagents with alkyl halides typically req...
Simple iron salts such as FeCln, Fe(acaC)(n) (n = 2,3) or the salen complex 4 turned out to be highl...
A new and efficient method for the synthesis of alkenyl iodides through direct coupling of alcohols ...
A novel iron-catalyzed hydrosilylation of alkenes process under solvent-free conditions has been rep...
Iron nanoparticles of size 6-16 nm have been successfully prepared by the reduction of FeCb with 3-p...
Iron(III) halides have proven to be excellent catalysts in the coupling of acetylenes and aldehydes....
A new robust methodology for gram-scale iron-catalyzed cross-coupling between alkyl Grignard reagent...
The first iron-catalyzed cross-coupling reaction of alkyl halides with alkylaluminum reagents (alkyl...
Iron-mediated sp-sp(3) C-C bond formation through the cross dehydrogenative coupling (CDC) of termin...
The stereoselective hydrogenation of alkynes constitutes one of the key approaches for the construct...
Aim of this thesis was the development of new iron-based catalyst systems for the hydrogenation of C...
The scope and mechanism of a practical protocol for the iron-catalyzed hydrogenation of alkenes and ...
Iron-catalysed carbonyl reduction, nitro reduction, formal hydroamination, and the radical alkenyla...
A new method for chlorination of alcohols and carboxylic acids, using α,α-dichlorodiphenylmethane as...
Cheap, readily available, air stable, nontoxic, and environmentally benign iron salts such as Fe(aca...
While attractive, the iron-catalyzed coupling of arylboron reagents with alkyl halides typically req...
Simple iron salts such as FeCln, Fe(acaC)(n) (n = 2,3) or the salen complex 4 turned out to be highl...
A new and efficient method for the synthesis of alkenyl iodides through direct coupling of alcohols ...
A novel iron-catalyzed hydrosilylation of alkenes process under solvent-free conditions has been rep...
Iron nanoparticles of size 6-16 nm have been successfully prepared by the reduction of FeCb with 3-p...
Iron(III) halides have proven to be excellent catalysts in the coupling of acetylenes and aldehydes....
A new robust methodology for gram-scale iron-catalyzed cross-coupling between alkyl Grignard reagent...
The first iron-catalyzed cross-coupling reaction of alkyl halides with alkylaluminum reagents (alkyl...
Iron-mediated sp-sp(3) C-C bond formation through the cross dehydrogenative coupling (CDC) of termin...
The stereoselective hydrogenation of alkynes constitutes one of the key approaches for the construct...
Aim of this thesis was the development of new iron-based catalyst systems for the hydrogenation of C...
The scope and mechanism of a practical protocol for the iron-catalyzed hydrogenation of alkenes and ...
Iron-catalysed carbonyl reduction, nitro reduction, formal hydroamination, and the radical alkenyla...
A new method for chlorination of alcohols and carboxylic acids, using α,α-dichlorodiphenylmethane as...
Cheap, readily available, air stable, nontoxic, and environmentally benign iron salts such as Fe(aca...
While attractive, the iron-catalyzed coupling of arylboron reagents with alkyl halides typically req...
Simple iron salts such as FeCln, Fe(acaC)(n) (n = 2,3) or the salen complex 4 turned out to be highl...