Brønsted acid-mediated annulation of carbazoles with diaryl-1,2-diones: access to furo[3,2- c ]carbazoles

Organic & Biomolecular Chemistry 2026

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Authors: Athira Kokkadan Subhash, Sachin Philip, Maarten Vlasselaer, Thanhchung Pham, Maxime Hodée, Daniel Escudero, Luc Van Meervelt, Wim Dehaen, SANTHINI V P V, Shandev P. P
DOI: 10.1039/d6ob00833j
Cited by: 1
References: 47

Abstract

]carbazoles was demonstrated through bromination, nitration, and formylation reactions. The synthesized compounds exhibited blue fluorescence with quantum yields of up to 77%, while photophysical, electrochemical, thermal, and computational studies provided insight into their electronic structures and excited-state properties.

Fields of Study & Subjects

Catalytic C–H Functionalization Methods Synthesis and pharmacology of benzodiazepine derivatives Catalytic Alkyne Reactions

Publication details

Journal / source
Organic & Biomolecular Chemistry
Publisher
Royal Society of Chemistry (RSC)
Volume
24
Issue
31
Pages
6452–6460
Publication date
1 January 2026
Language
EN