Appropriately substituted 2-alkenylphenols undergo a mild formal [3C+2C] cycloaddition with alkynes when treated with a Rh(III) catalyst and an oxidant. The reaction, which involves the cleavage of the terminal C–H bond of the alkenyl moiety and the dearomatization of the phenol ring, provides a versatile and efficient approach to highly appealing spirocyclic skeletons and occurs with high selectivity
A unique Rh(III)-catalyzed oxidative [5 + 2] annulation of easily available 2-alkenylphenols with p...
The development of the rhodium-catalyzed [(3+2)+1] carbocyclization reaction of alkynylidenecyclo...
A new, one-step rhodium(III)-catalyzed annulation of 4-arylbut-3-yn-1-amines with internal alkynes ...
Appropriately substituted 2-alkenylphenols undergo a mild formal [3C+2C] cycloaddition with alkyne...
Rh(III) catalysts can promote a formal (4 + 2) intramolecular oxidative annulation between acrylic ...
Nitrogen-rich heterocyclic compounds have a profound impact on human health. Despite the numerous sy...
Nitrogen-rich heterocyclic compounds have a profound impact on human health. Despite the numerous sy...
The dearomatizing oxidative annulation of 2-alkenylphenols with alkynes and enynes proceeds with hig...
The dearomatizing oxidative annulation of 2-alkenylphenols with alkynes and enynes proceeds with hig...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
A novel Rh-catalyzed carbonylative [3 + 2 + 1] cycloaddition of alkyne-tethered alkylidenecyclopro...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
The development of the rhodium-catalyzed [(3+2)+1] carbocyclization reaction of alkynylidenecyclo...
A Rh-catalyzed enol-directed formal sp<sup>3</sup> C–H activation/annulation of α-arylidene pyrazolo...
By using an oxidizing directing group, a mild, efficient Rh(III) catalyzed C–H olefination reaction ...
A unique Rh(III)-catalyzed oxidative [5 + 2] annulation of easily available 2-alkenylphenols with p...
The development of the rhodium-catalyzed [(3+2)+1] carbocyclization reaction of alkynylidenecyclo...
A new, one-step rhodium(III)-catalyzed annulation of 4-arylbut-3-yn-1-amines with internal alkynes ...
Appropriately substituted 2-alkenylphenols undergo a mild formal [3C+2C] cycloaddition with alkyne...
Rh(III) catalysts can promote a formal (4 + 2) intramolecular oxidative annulation between acrylic ...
Nitrogen-rich heterocyclic compounds have a profound impact on human health. Despite the numerous sy...
Nitrogen-rich heterocyclic compounds have a profound impact on human health. Despite the numerous sy...
The dearomatizing oxidative annulation of 2-alkenylphenols with alkynes and enynes proceeds with hig...
The dearomatizing oxidative annulation of 2-alkenylphenols with alkynes and enynes proceeds with hig...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
A novel Rh-catalyzed carbonylative [3 + 2 + 1] cycloaddition of alkyne-tethered alkylidenecyclopro...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
The development of the rhodium-catalyzed [(3+2)+1] carbocyclization reaction of alkynylidenecyclo...
A Rh-catalyzed enol-directed formal sp<sup>3</sup> C–H activation/annulation of α-arylidene pyrazolo...
By using an oxidizing directing group, a mild, efficient Rh(III) catalyzed C–H olefination reaction ...
A unique Rh(III)-catalyzed oxidative [5 + 2] annulation of easily available 2-alkenylphenols with p...
The development of the rhodium-catalyzed [(3+2)+1] carbocyclization reaction of alkynylidenecyclo...
A new, one-step rhodium(III)-catalyzed annulation of 4-arylbut-3-yn-1-amines with internal alkynes ...