A Rh(II)-catalyzed transannulation of <i>N</i>-sulfonyl-1,2,3-triazoles with 2,1-benzisoxazoles has been developed, which affords an efficient method for the synthesis of quinazoline derivatives. The transformation represents an unprecedented example which utilizes <i>N</i>-sulfonyl-1,2,3-triazole as an aza-[2C]-component in cycloadditions. Meanwhile, a Rh(II)-catalyzed formal [3 + 2] cycloaddition of <i>N</i>-sulfonyl-1,2,3-triazoles with 1,2-benzisoxazoles is also presented, which enables the rapid synthesis of functionalized imidazole derivatives
Readily available 1-mesyl-1,2,3-triazoles are efficiently converted into a variety of imidazolones a...
The rhodium(III)-catalyzed C–H functionalization followed by intramolecular annulation reactions be...
A Rh(II)-catalyzed dearomative intramolecular [3 + 2] dipolar cycloaddition involving the indolic C2...
A novel rhodium(II)-catalyzed formal [3 + 2] cycloaddition of <i>N</i>-sulfonyl-1,2,3-triazoles wit...
An efficient, Rh(II)-catalyzed, denitrogenative reaction of 4-vinyl benzoxazinanones with N-sulfony...
An effective method for the synthesis of fully substituted 5-sulfonamidoimidazoles by Rh(II)-cataly...
An efficient, Rh(II)-catalyzed, denitrogenative reaction of 4-vinyl benzoxazinanones with N-sulfonyl...
A facile rhodium-catalyzed transannulation of 1-sulfonyl-1,2,3-triazoles with β-diketones was realiz...
α-Imino carbenes generated from N-sulfonyl-1,2,3-triazoles undergo many original processes, from cyc...
A synthetic method for 2-bromoimidazoles is developed from Rh-catalyzed cyclization of <i>N</i>-sulf...
An efficient and novel rhodium-catalyzed transannulation of <i>N</i>-sulfonyl-1,2,3-triazoles with i...
An efficient protocol to synthesize substituted benzo[4,5]imidazo[1,2-c]quinazolines starting fr...
A regiodivergent Rh(I)-catalyzed azide–alkyne cycloaddition (RhAAC) was developed for the synthesis...
Rhodium(II) acetate catalyzes the denitrogenative transformation of 4-substituted 1-sulfonyl-1,2,3-...
A convenient and simple, Rh-II-catalyzed denitrogenative method for the synthesis of biologically in...
Readily available 1-mesyl-1,2,3-triazoles are efficiently converted into a variety of imidazolones a...
The rhodium(III)-catalyzed C–H functionalization followed by intramolecular annulation reactions be...
A Rh(II)-catalyzed dearomative intramolecular [3 + 2] dipolar cycloaddition involving the indolic C2...
A novel rhodium(II)-catalyzed formal [3 + 2] cycloaddition of <i>N</i>-sulfonyl-1,2,3-triazoles wit...
An efficient, Rh(II)-catalyzed, denitrogenative reaction of 4-vinyl benzoxazinanones with N-sulfony...
An effective method for the synthesis of fully substituted 5-sulfonamidoimidazoles by Rh(II)-cataly...
An efficient, Rh(II)-catalyzed, denitrogenative reaction of 4-vinyl benzoxazinanones with N-sulfonyl...
A facile rhodium-catalyzed transannulation of 1-sulfonyl-1,2,3-triazoles with β-diketones was realiz...
α-Imino carbenes generated from N-sulfonyl-1,2,3-triazoles undergo many original processes, from cyc...
A synthetic method for 2-bromoimidazoles is developed from Rh-catalyzed cyclization of <i>N</i>-sulf...
An efficient and novel rhodium-catalyzed transannulation of <i>N</i>-sulfonyl-1,2,3-triazoles with i...
An efficient protocol to synthesize substituted benzo[4,5]imidazo[1,2-c]quinazolines starting fr...
A regiodivergent Rh(I)-catalyzed azide–alkyne cycloaddition (RhAAC) was developed for the synthesis...
Rhodium(II) acetate catalyzes the denitrogenative transformation of 4-substituted 1-sulfonyl-1,2,3-...
A convenient and simple, Rh-II-catalyzed denitrogenative method for the synthesis of biologically in...
Readily available 1-mesyl-1,2,3-triazoles are efficiently converted into a variety of imidazolones a...
The rhodium(III)-catalyzed C–H functionalization followed by intramolecular annulation reactions be...
A Rh(II)-catalyzed dearomative intramolecular [3 + 2] dipolar cycloaddition involving the indolic C2...