One‐step syntheses of carbocycles substituted with amines from simple starting materials remain rare. We recently developed an intermolecular [3+2] annulation of cyclopropylanilines with alkenes and alkynes that enables this one‐step synthesis. Herein, we report our findings for a full‐scale study of the annulation. Significant expansion of the substrate scope for both cyclopropylanilines and alkynes has been achieved. A range of structurally diverse carbocycles substituted with amines is prepared
Cascade reactions represent a class of ideal organic reactions because they empower efficiency, eleg...
The visible-light-promoted activation of conjugated C-C double bonds is well developed, while that o...
Amino alcohols, cyclopropanes and nitriles are privileged structural motifs found in the scaffold of...
Intermolecular [3 + 2] annulation of cyclopropylanilines with alkynes is realized using visible ligh...
We report the first example of an intermolecular [4+2] annulation of cyclobutylanilines with alkynes...
Over the past decade, pharmaceutical industries have prioritized their focus on discovering new inno...
Visible light photocatalysis has emerged as a powerful tool in organic synthesis. The formation of r...
UV-activated alkyne-alkene [2+2] cycloaddition has served as an important tool to access cyclobutene...
Here is the first visible light catalytic intermolecular cross [2 + 2] cycloaddition of enynes with ...
A photoinduced copper-catalyzed three-component reaction involving carbohalide, alkene and amine has...
We report a visible-light-promoted synthesis of substituted naphthalenes via [4 + 2] annulation of a...
Continuous flow has recently emerged as a powerful enabling technology that greatly improves many re...
We report herein a novel photocyclopropanation of dibromomalonates with alkenes in the presence of H...
Embedded medium-sized carbacycles and cyclohepta [b] indoles occur frequently as scaffold elements i...
We herein report a phosphine-catalyzed (3 + 2) annulation of cyclopropenones with a wide variety of ...
Cascade reactions represent a class of ideal organic reactions because they empower efficiency, eleg...
The visible-light-promoted activation of conjugated C-C double bonds is well developed, while that o...
Amino alcohols, cyclopropanes and nitriles are privileged structural motifs found in the scaffold of...
Intermolecular [3 + 2] annulation of cyclopropylanilines with alkynes is realized using visible ligh...
We report the first example of an intermolecular [4+2] annulation of cyclobutylanilines with alkynes...
Over the past decade, pharmaceutical industries have prioritized their focus on discovering new inno...
Visible light photocatalysis has emerged as a powerful tool in organic synthesis. The formation of r...
UV-activated alkyne-alkene [2+2] cycloaddition has served as an important tool to access cyclobutene...
Here is the first visible light catalytic intermolecular cross [2 + 2] cycloaddition of enynes with ...
A photoinduced copper-catalyzed three-component reaction involving carbohalide, alkene and amine has...
We report a visible-light-promoted synthesis of substituted naphthalenes via [4 + 2] annulation of a...
Continuous flow has recently emerged as a powerful enabling technology that greatly improves many re...
We report herein a novel photocyclopropanation of dibromomalonates with alkenes in the presence of H...
Embedded medium-sized carbacycles and cyclohepta [b] indoles occur frequently as scaffold elements i...
We herein report a phosphine-catalyzed (3 + 2) annulation of cyclopropenones with a wide variety of ...
Cascade reactions represent a class of ideal organic reactions because they empower efficiency, eleg...
The visible-light-promoted activation of conjugated C-C double bonds is well developed, while that o...
Amino alcohols, cyclopropanes and nitriles are privileged structural motifs found in the scaffold of...