The development of a new method for the assembly of unsymmetrical carbazoles is
reported. The strategy involves the selective intramolecular functionalization of an arene CH …

Highly convergent syntheses of substituted carbazoles are most conveniently achieved
using organometallic chemistry. Construction of the carbazole framework via the iron …

A new method in which a series of substituted carbazoles is efficiently produced by the
combination of an amide and an arene is described. The key feature of this method is the …

A novel catalytic one-pot synthesis of carbazoles via consecutive amination and C–H
activation - Chemical Communications (RSC Publishing) DOI:10.1039/B207712B Royal …

An efficient catalytic system has been developed for the synthesis of carbazoles by one-pot
N-arylation and oxidative biaryl coupling. A significant substituent effect of the diarylamine …

An efficient indole-to-carbazole strategy has been developed under metal-free conditions.
This carbazole formation was highly promoted by NH4I with high regioselectivity through …

The carbazole nucleus is a predominant feature of a vast array of heterocyclic compounds. It
occurs in naturally occurring alkaloids, optoelectronic materials, and anion-binding ligands …

Substituted carbazoles are readily prepared in good yields by the palladium-catalyzed cross-
coupling of alkynes and N-(3-iodophenyl) anilines. This process proceeds by …

Two sequential palladium-catalyzed reactions are the key steps in a novel synthetic route to
carbazolones, an intermolecular Stille coupling followed by a recently developed palladium …

A new efficient synthesis of indolo [3, 2, 1-jk] carbazoles by the palladium-catalyzed
cyclization of N-(2-bromoaryl) carbazoles is described. The reaction involves intramolecular …