Readily available 1-mesyl-1,2,3-triazoles are efficiently converted into a variety of imidazolones and thiazoles by Rh(II)-catalyzed denitrogenative reactions with isocyanates and isothiocyanates, respectively. The proposed triazole–diazoimine equilibrium results in the formation of highly reactive azavinyl metal-carbenes, which react with heterocumulenes causing an apparent swap of 1,2,3-triazole core for another heterocycle
Triazolylidenes have rapidly emerged as a powerful subclass of N-heterocyclic carbene ligands for tr...
In the presence of a Rh(II) catalyst and β-(methylthio)-α,β-unsaturated ketones, 1-sulfonyl-1,2,3-t...
1,2,3-Triazoles are unique heterocycles with intriguing physical properties that allow not only the ...
A synthetic method for obtaining a wide variety of isothiazoles by the Rh-catalyzed transannulation ...
This highlight solely focusses on the synthetic applications of azavinyl rhodium(II) carbenes derive...
This highlight solely focusses on the synthetic applications of azavinyl rhodium(II) carbenes derive...
α-Imino carbenes generated from N-sulfonyl-1,2,3-triazoles undergo many original processes, from cyc...
A rhodium(II)-catalyzed denitrogenative coupling of <i>N</i>-sulfonyl-1,2,3-triazoles with ambiphil...
An alternative entry to transformations of <i>N</i>-sulfonyl-4-(2-(ethynyl)aryl)-1,2,3-triazoles wi...
Treatment of N-heterocyclic carbenes (as their free carbenes or generated in situ) with alkyl, aryl,...
Herein, we disclose substrate-dependent rearrangements of 4-substituted N-sulfonyl-1,2,3-triazoles u...
An effective method for the synthesis of fully substituted 5-sulfonamidoimidazoles by Rh(II)-cataly...
A Rh(II)-catalyzed transannulation of <i>N</i>-sulfonyl-1,2,3-triazoles with 2,1-benzisoxazoles has...
The higher propensity of C–N over C–S bond forming ability was demonstrated, through formal C–H func...
Copyright © 2013 Aldo I. Ortega-Arizmendi et al. This is an open access article distributed under th...
Triazolylidenes have rapidly emerged as a powerful subclass of N-heterocyclic carbene ligands for tr...
In the presence of a Rh(II) catalyst and β-(methylthio)-α,β-unsaturated ketones, 1-sulfonyl-1,2,3-t...
1,2,3-Triazoles are unique heterocycles with intriguing physical properties that allow not only the ...
A synthetic method for obtaining a wide variety of isothiazoles by the Rh-catalyzed transannulation ...
This highlight solely focusses on the synthetic applications of azavinyl rhodium(II) carbenes derive...
This highlight solely focusses on the synthetic applications of azavinyl rhodium(II) carbenes derive...
α-Imino carbenes generated from N-sulfonyl-1,2,3-triazoles undergo many original processes, from cyc...
A rhodium(II)-catalyzed denitrogenative coupling of <i>N</i>-sulfonyl-1,2,3-triazoles with ambiphil...
An alternative entry to transformations of <i>N</i>-sulfonyl-4-(2-(ethynyl)aryl)-1,2,3-triazoles wi...
Treatment of N-heterocyclic carbenes (as their free carbenes or generated in situ) with alkyl, aryl,...
Herein, we disclose substrate-dependent rearrangements of 4-substituted N-sulfonyl-1,2,3-triazoles u...
An effective method for the synthesis of fully substituted 5-sulfonamidoimidazoles by Rh(II)-cataly...
A Rh(II)-catalyzed transannulation of <i>N</i>-sulfonyl-1,2,3-triazoles with 2,1-benzisoxazoles has...
The higher propensity of C–N over C–S bond forming ability was demonstrated, through formal C–H func...
Copyright © 2013 Aldo I. Ortega-Arizmendi et al. This is an open access article distributed under th...
Triazolylidenes have rapidly emerged as a powerful subclass of N-heterocyclic carbene ligands for tr...
In the presence of a Rh(II) catalyst and β-(methylthio)-α,β-unsaturated ketones, 1-sulfonyl-1,2,3-t...
1,2,3-Triazoles are unique heterocycles with intriguing physical properties that allow not only the ...