The azido group is found in large numbers of natural products, drugs, biochemicals and materials and to date, many elegant and useful methods for the synthesis of organic azides and their transformations have been documented. In this review, we provide a summary of the state of the art of radical azidation for the construction of C(sp3)-N3 bonds. There is a specific emphasis on the synthetic reactions involving C(sp3)-H azidation, decarboxylative azidation and difunctionalized azidation of olefins. This review will be useful to those working in this field and hopefully could inspire further development of radical azidation reactions
Mn(iii)-catalyzed formal [3+2]- and [3+3]-annulations have been developed using readily available vi...
© 2017 Dr Emma Catherine ReadThis thesis is concerned with intermolecular radical addition reactions...
Selective functionalization of complex scaffolds is a promising approach to alter the pharmacologica...
A wide range of methodologies for the preparation of organic azides has been reported in the literat...
Recent advances in radical azidation using sulfonyl azides are presented. For instance, radical carb...
Dichloroindium hydride revealed to be a valid alternative to tributyltin hydride for radical reduct...
Organic azides are key motifs in compounds of relevance to chemical biology, medicinal chemistry and...
An in-depth study of the mechanism of the azidation of C(sp3)-H bonds with Zhdankin's λ3-azidoiodane...
This feature article provides an overview of the application of organic azides for the intermolecula...
A persulfate induced radical process to transform aliphatic tertiary C-H bonds into organic azides u...
The azide moiety is a desirable functionality in organic molecules, useful in a variety of transform...
Radical azidooxygenation of various alkenes is described. A readily prepared N<sub>3</sub>-iodine(II...
The azido group occupies an important position in modern organic chemistry, broadly used as amine su...
The γ-nitrogen of phenylsulfonyl azide can be readily labeled with 15N by treating benzenesulfonyl ...
none3Over the last thirty years organic azides have drawn a great deal of attention as radical trap...
Mn(iii)-catalyzed formal [3+2]- and [3+3]-annulations have been developed using readily available vi...
© 2017 Dr Emma Catherine ReadThis thesis is concerned with intermolecular radical addition reactions...
Selective functionalization of complex scaffolds is a promising approach to alter the pharmacologica...
A wide range of methodologies for the preparation of organic azides has been reported in the literat...
Recent advances in radical azidation using sulfonyl azides are presented. For instance, radical carb...
Dichloroindium hydride revealed to be a valid alternative to tributyltin hydride for radical reduct...
Organic azides are key motifs in compounds of relevance to chemical biology, medicinal chemistry and...
An in-depth study of the mechanism of the azidation of C(sp3)-H bonds with Zhdankin's λ3-azidoiodane...
This feature article provides an overview of the application of organic azides for the intermolecula...
A persulfate induced radical process to transform aliphatic tertiary C-H bonds into organic azides u...
The azide moiety is a desirable functionality in organic molecules, useful in a variety of transform...
Radical azidooxygenation of various alkenes is described. A readily prepared N<sub>3</sub>-iodine(II...
The azido group occupies an important position in modern organic chemistry, broadly used as amine su...
The γ-nitrogen of phenylsulfonyl azide can be readily labeled with 15N by treating benzenesulfonyl ...
none3Over the last thirty years organic azides have drawn a great deal of attention as radical trap...
Mn(iii)-catalyzed formal [3+2]- and [3+3]-annulations have been developed using readily available vi...
© 2017 Dr Emma Catherine ReadThis thesis is concerned with intermolecular radical addition reactions...
Selective functionalization of complex scaffolds is a promising approach to alter the pharmacologica...