2,2-Diiodo-5,5-dimethylcyclohexane-1,3-dione is reported as a new electrophilic iodinating agent that selectively iodinates electron-rich aromatics. In contrast to other common electrophilic iodinating reagents, its mild nature allows it to be used for the selective synthesis of alpha-iodinated carbonyl compounds from allylic alcohols through a 1,3-hydrogen shift/iodination process catalyzed by iridium(III) complexes
The reaction of (Z) Methyl-ß-iodo propenoate with diisobutylaluminium hydride and subsequent reactio...
alpha-Brominated ketones and aldehydes, with two adjacent electrophilic carbon atoms, are highly val...
Iodoarenes are versatile intermediates and common synthetic targets in organic synthesis. Here, we p...
2,2-Diiodo-5,5-dimethylcyclohexane-1,3-dione is reported as a new electrophilic iodinating agent tha...
An efficient method for the synthesis of alpha-iodoketones from allylic alcohols and elemental iodin...
The general synthesis, isolation and characterization of electrophilic iodine reagents of the genera...
Herein, a disulfide-catalyzed electrophilic iodination of aromatic compounds using 1,3-diiodo-5,5-di...
Aryl iodides are important synthetic intermediates that can be transformed into tritium labelled com...
Lodine was efficiently introduced into the methoxy substituted aromatic compounds, acetophenone, 1-i...
An oxidative procedure for the electrophilic iodination of phenols was developed by using iodosylben...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
Hypervalent iodine reagents are environmentally benign alternatives to heavy metal oxidants. They a...
This thesis discloses two different applications of hypervalent iodine(III) reagents in organic synt...
The selective synthesis of a-functionalized ketones with two similar enolizable positions can be acc...
702-703A direct iodination procedure is described for the introduction of iodine in the 3-position o...
The reaction of (Z) Methyl-ß-iodo propenoate with diisobutylaluminium hydride and subsequent reactio...
alpha-Brominated ketones and aldehydes, with two adjacent electrophilic carbon atoms, are highly val...
Iodoarenes are versatile intermediates and common synthetic targets in organic synthesis. Here, we p...
2,2-Diiodo-5,5-dimethylcyclohexane-1,3-dione is reported as a new electrophilic iodinating agent tha...
An efficient method for the synthesis of alpha-iodoketones from allylic alcohols and elemental iodin...
The general synthesis, isolation and characterization of electrophilic iodine reagents of the genera...
Herein, a disulfide-catalyzed electrophilic iodination of aromatic compounds using 1,3-diiodo-5,5-di...
Aryl iodides are important synthetic intermediates that can be transformed into tritium labelled com...
Lodine was efficiently introduced into the methoxy substituted aromatic compounds, acetophenone, 1-i...
An oxidative procedure for the electrophilic iodination of phenols was developed by using iodosylben...
Aryl iodides have become widely recognized as versatile synthetic intermediates, owing to aromatic i...
Hypervalent iodine reagents are environmentally benign alternatives to heavy metal oxidants. They a...
This thesis discloses two different applications of hypervalent iodine(III) reagents in organic synt...
The selective synthesis of a-functionalized ketones with two similar enolizable positions can be acc...
702-703A direct iodination procedure is described for the introduction of iodine in the 3-position o...
The reaction of (Z) Methyl-ß-iodo propenoate with diisobutylaluminium hydride and subsequent reactio...
alpha-Brominated ketones and aldehydes, with two adjacent electrophilic carbon atoms, are highly val...
Iodoarenes are versatile intermediates and common synthetic targets in organic synthesis. Here, we p...