An efficient ligand-free iron-catalyzed cross-coupling reaction involving alkenyllithium and vinyl iodides was developed to form diene species in moderate to good yields. This new iron-catalyzed cross-coupling reaction provides a mild, inexpensive, and environmentally friendly avenue toward synthesis of diversified diene derivatives
Transition metal catalysts, particularly those derived from the group VIII−X metals, display remarka...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
An operationally simple iron-catalyzed reductive cross-coupling reaction between aryl halides and al...
An efficient synthetic protocol involving iron-catalyzed cross-coupling reactions between organolith...
(Chemical Equation Presented) An efficient and ligand-free C-N cross-coupling of aryl halides with v...
A new strategy was developed for the efficient synthesis of di-, tetra-, and hexa-substituted 1,3-bu...
This account summarizes recent developments in the use of cheap, benign, and non-toxic iron salts as...
This account summarizes recent developments in the use of cheap, benign, and non-toxic iron salts as...
The first iron-catalyzed cross-coupling reaction of alkyl halides with alkylaluminum reagents (alkyl...
Structurally diverse 1,3-dienes are valuable building blocks in organic synthesis. Herein we report ...
Cheap, readily available, air stable, nontoxic, and environmentally benign iron salts such as Fe(aca...
Iron-mediated sp-sp(3) C-C bond formation through the cross dehydrogenative coupling (CDC) of termin...
This Article details the development of the iron-catalyzed conversion of olefins to radicals and the...
This Article details the development of the iron-catalyzed conversion of olefins to radicals and the...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
Transition metal catalysts, particularly those derived from the group VIII−X metals, display remarka...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
An operationally simple iron-catalyzed reductive cross-coupling reaction between aryl halides and al...
An efficient synthetic protocol involving iron-catalyzed cross-coupling reactions between organolith...
(Chemical Equation Presented) An efficient and ligand-free C-N cross-coupling of aryl halides with v...
A new strategy was developed for the efficient synthesis of di-, tetra-, and hexa-substituted 1,3-bu...
This account summarizes recent developments in the use of cheap, benign, and non-toxic iron salts as...
This account summarizes recent developments in the use of cheap, benign, and non-toxic iron salts as...
The first iron-catalyzed cross-coupling reaction of alkyl halides with alkylaluminum reagents (alkyl...
Structurally diverse 1,3-dienes are valuable building blocks in organic synthesis. Herein we report ...
Cheap, readily available, air stable, nontoxic, and environmentally benign iron salts such as Fe(aca...
Iron-mediated sp-sp(3) C-C bond formation through the cross dehydrogenative coupling (CDC) of termin...
This Article details the development of the iron-catalyzed conversion of olefins to radicals and the...
This Article details the development of the iron-catalyzed conversion of olefins to radicals and the...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
Transition metal catalysts, particularly those derived from the group VIII−X metals, display remarka...
An iron-catalyzed cross-coupling reaction between alkyl halides and arylboronic esters was developed...
An operationally simple iron-catalyzed reductive cross-coupling reaction between aryl halides and al...