The first iron-catalyzed cross-coupling reaction of alkyl halides with alkylaluminum reagents (alkyl–alkyl Negishi coupling) is developed using an iron/bisphosphine catalyst system. The reaction shows high functional group tolerance: various primary alkyl halides possessing a non-protected indole, carboxyl, or hydroxy group are coupled with primary alkylaluminum reagents in good yields. Potassium fluoride plays a key role to promote the reaction by generating an aluminate species, which facilitates the transmetalation between the organoaluminum and the iron catalyst
Transition metal catalysts, particularly those derived from the group VIII−X metals, display remarka...
Aryl chlorides are better substrates than the corresponding bromides or iodides in the presented cro...
Cheap, readily available, air stable, nontoxic, and environmentally benign iron salts such as Fe(aca...
We report the first example of iron-catalyzed cross-coupling of α-halo-β,β-difluoroethylene-containi...
A simple protocol for iron-catalyzed cross-coupling of nonactivated secondary alkyl bromides and iod...
Although iron-catalyzed cross-coupling reactions of arylmagnesium halides with alkyl halides are wel...
International audienceIron catalysis has raised a great interest in the organometallic field since t...
International audienceIron catalysis has raised a great interest in the organometallic field since t...
International audienceIron catalysis has raised a great interest in the organometallic field since t...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
A stereospecific and high-yielding cross-coupling reaction between alkenylboron reagents and alkyl h...
1 - ArticleAny old iron: Two efficient iron-catalyzed cross-coupling reactions between aryl Grignard...
While attractive, the iron-catalyzed coupling of arylboron reagents with alkyl halides typically req...
Transition metal catalysts, particularly those derived from the group VIII−X metals, display remarka...
Transition metal catalysts, particularly those derived from the group VIII−X metals, display remarka...
Aryl chlorides are better substrates than the corresponding bromides or iodides in the presented cro...
Cheap, readily available, air stable, nontoxic, and environmentally benign iron salts such as Fe(aca...
We report the first example of iron-catalyzed cross-coupling of α-halo-β,β-difluoroethylene-containi...
A simple protocol for iron-catalyzed cross-coupling of nonactivated secondary alkyl bromides and iod...
Although iron-catalyzed cross-coupling reactions of arylmagnesium halides with alkyl halides are wel...
International audienceIron catalysis has raised a great interest in the organometallic field since t...
International audienceIron catalysis has raised a great interest in the organometallic field since t...
International audienceIron catalysis has raised a great interest in the organometallic field since t...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
A stereospecific and high-yielding cross-coupling reaction between alkenylboron reagents and alkyl h...
1 - ArticleAny old iron: Two efficient iron-catalyzed cross-coupling reactions between aryl Grignard...
While attractive, the iron-catalyzed coupling of arylboron reagents with alkyl halides typically req...
Transition metal catalysts, particularly those derived from the group VIII−X metals, display remarka...
Transition metal catalysts, particularly those derived from the group VIII−X metals, display remarka...
Aryl chlorides are better substrates than the corresponding bromides or iodides in the presented cro...
Cheap, readily available, air stable, nontoxic, and environmentally benign iron salts such as Fe(aca...