The interest of scientists in the carbazole core has risen steadily over the last 30 years,
particularly over the last decade given its presence in several active pharmaceutical …

This article demonstrates recent innovative cascade annulation methods for preparing
functionalized carbazoles and their related polyaromatic heterocyclic compounds enabled …

A method for the regioselective functionalization of haloarenes through deprotonative
lithiation is disclosed. The generated haloaryllithiums were trapped in a batch reactor with a …

A new, one-pot domino benzannulation reaction between indole-3-ynones and various
nitromethane derivatives has been explored for a general entry to diversely functionalized …

The transition-metal-free total syntheses of the oxygenated carbazole natural products
glycoborine, carbazomycin A and carbazomycin B are reported. The key step involves an …

A new one-step, reagent-directed regioselective synthesis of chirally enriched
tetrahydrocarbazolones and tetrahydrocarbazoles from a common type of substrate has …

The exploration of a ring expansion reaction from indole cyclopentanone to generate a
range of diversely functionalized 4-hydroxyl carbazole frameworks, representing the core …

Diels‐Alder reaction is one of the most well‐known named reactions in organic chemistry. It
involves a diene substrate and a dienophile substrate. Among dienes, siloxydiene is a …

Two series of carbazole analogs of 8‐methoxy‐N‐substituted‐9H‐carbazole‐3‐
carboxamides (series 1) and carbazolyl substituted rhodanines (series 2) were synthesized …

Lanthanide triflates and a series of hexadentate chiral ligand complexes were synthesized.
X‐ray‐quality crystals were obtained from mixtures of the lanthanide complexes, which were …