α-Azidochalcones were coupled with 1/2-naphthols or 2-hydroxy-1,4-naphthoquinone using Ru(bpy)3(PF6)2 as a photocatalyst under blue LED light irradiation to yield 2,3-fused pyrroles in high yields (68–84%). The overall transformation involves photosensitized decomposition of α-azidochalcones into highly reactive 2H-azirines which are trapped by 1/2-naphthols or 2-hydroxy-1,4-naphthoquinone, leading to the construction of two new C–N and one new C–C bonds
The synthesis of 1,3,4-trisubstituted pyrroles via visible-light mediated photoredox catalyzed conde...
Free carbenes generated from α-diazo oxime ethers by photolysis undergo facile N–O insertion to affo...
We report a one-step procedure for the preparation of N-(2-pyrrole)-sulfonamides from sulfonamides a...
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tri...
1-(2-Bromophenyl)-1H-pyrrole and 1-(2,6-dibromophenyl)-1H-pyrrole react in the presence of catalytic...
The preparation of 2-(3-pyrrolin-1-yl)-1,4-naphthoquinones and a study of their use as photoactivate...
The photoredox-catalyzed coupling of <i>N</i>-aryltetrahydroisoquinoline and Michael acceptors was a...
The photoredox-catalyzed coupling of <i>N</i>-aryltetrahydroisoquinoline and Michael acceptors was a...
The photoredox-catalyzed coupling of <i>N</i>-aryltetrahydroisoquinoline and Michael acceptors was a...
The photoredox-catalyzed coupling of <i>N</i>-aryltetrahydroisoquinoline and Michael acceptors was a...
Herein, we document the design and development of a novel (3 + 2) cycloaddition reaction aided by th...
Three isoelectronic analogues of pyrido[2,1-<i>a</i>]isoindole have been found to undergo a facile...
Free carbenes generated from ??-diazo oxime ethers by photolysis undergo facile N-O insertion to aff...
A facile three-step approach to synthesizing quinoline-fused pyrrolopyrroles is reported. The crucia...
A facile three-step approach to synthesizing quinoline-fused pyrrolopyrroles is reported. The crucia...
The synthesis of 1,3,4-trisubstituted pyrroles via visible-light mediated photoredox catalyzed conde...
Free carbenes generated from α-diazo oxime ethers by photolysis undergo facile N–O insertion to affo...
We report a one-step procedure for the preparation of N-(2-pyrrole)-sulfonamides from sulfonamides a...
Use of FEP flow reactor technology allows access to gram quantities of photochemically-generated tri...
1-(2-Bromophenyl)-1H-pyrrole and 1-(2,6-dibromophenyl)-1H-pyrrole react in the presence of catalytic...
The preparation of 2-(3-pyrrolin-1-yl)-1,4-naphthoquinones and a study of their use as photoactivate...
The photoredox-catalyzed coupling of <i>N</i>-aryltetrahydroisoquinoline and Michael acceptors was a...
The photoredox-catalyzed coupling of <i>N</i>-aryltetrahydroisoquinoline and Michael acceptors was a...
The photoredox-catalyzed coupling of <i>N</i>-aryltetrahydroisoquinoline and Michael acceptors was a...
The photoredox-catalyzed coupling of <i>N</i>-aryltetrahydroisoquinoline and Michael acceptors was a...
Herein, we document the design and development of a novel (3 + 2) cycloaddition reaction aided by th...
Three isoelectronic analogues of pyrido[2,1-<i>a</i>]isoindole have been found to undergo a facile...
Free carbenes generated from ??-diazo oxime ethers by photolysis undergo facile N-O insertion to aff...
A facile three-step approach to synthesizing quinoline-fused pyrrolopyrroles is reported. The crucia...
A facile three-step approach to synthesizing quinoline-fused pyrrolopyrroles is reported. The crucia...
The synthesis of 1,3,4-trisubstituted pyrroles via visible-light mediated photoredox catalyzed conde...
Free carbenes generated from α-diazo oxime ethers by photolysis undergo facile N–O insertion to affo...
We report a one-step procedure for the preparation of N-(2-pyrrole)-sulfonamides from sulfonamides a...