4.6 Article

Preparation of Carbazoles Involving 6π-Electrocyclization, Photoredox-, Electrochemical-, and Thermal Cyclization Reactions: Mechanistic Insights

Related references

Note: Only part of the references are listed.
Article Chemistry, Organic

Synthesis of C4-Aminated Carbazoles and Their Derivatives via Pd/NBE Chemistry

Bo-Sheng Zhang et al.

Summary: This report presents a one-step synthesis of C4-aminated carbazoles and their derivatives through a series reaction of C-H amination and arylation. The substrate scope is wide, allowing for the synthesis of C4-amino carbazoles substituted by C2, C6, C7, and C8 methyl groups, as well as carbazole derivatives of fused rings, pyridine, and dibenzofuran.

JOURNAL OF ORGANIC CHEMISTRY (2023)

Review Chemistry, Physical

Construction of Benzo-Fused Polycyclic Heteroaromatic Compounds through Palladium-Catalyzed Intramolecular C-H/C-H Biaryl Coupling

Yuji Nishii et al.

Summary: Dibenzo-fused five-membered heteroaromatic compounds, such as dibenzofuran, carbazole, and dibenzothiophene, are important structural units in various polycyclic heteroaromatic compounds. The intramolecular C-H/C-H biaryl coupling of diaryl (thio)ethers and amines based on palladium(II) catalysis under oxidative conditions is an effective method for their construction. This mini-review briefly summarizes representative examples of constructing structurally intriguing pi-extended polycyclic heteroaromatics through catalytic coupling reactions.

CATALYSTS (2023)

Review Chemistry, Multidisciplinary

LNL-Carbazole Pincer Ligand: More than the Sum of Its Parts

George Kleinhans et al.

Summary: This review aims to systematically explore and illustrate the key features of the LNL-carbazolide binding to transition metal centers and the significant benefits that can be obtained from it. It highlights the potential of the ligand design strategies in functional molecules for various applications such as stereoselective catalysis, small molecule activation, SET and redox applications, and chemotherapeutics. The versatile pincer assembly shows promise not only for transition metals but also for s-, p-, and f-block elements.

CHEMICAL REVIEWS (2023)

Article Chemistry, Multidisciplinary

Iron-catalyzed reductive cyclization of nitroarenes: Synthesis of aza-heterocycles and DFT calculations

Christine Tran et al.

Summary: We developed a new approach for synthesizing substituted dihydrobenzo[c]carbazoles and indoles through iron-catalyzed hydrogen transfer reduction of nitroarenes followed by intramolecular cyclization. This strategy involves the use of a Knolker-type catalyst, Cs2CO3 as the base, and benzyl alcohol as the hydrogen donor. We synthesized 30 examples of aza-heterocycles with moderate to excellent yields using this approach. DFT calculations suggest an anionic mechanism for the reaction pathway.

CHINESE CHEMICAL LETTERS (2023)

Article Chemistry, Organic

Solvent Effects on the Photoinduced [6?]-Electrocyclization Reactions of Mono-, Di-, and Trisubstituted Arylamines: Photophysical, Preparative Photochemistry, and Mechanistic Investigations

Ivan E. Romero et al.

Summary: This study investigates the effects of substituents and solvents on the spectroscopic behavior and the photoinduced [6x]-electro-cyclization reaction of substituted triphenylamine derivatives. It is found that triphenylamines with electron-donor substituents produce substituted exo/endo carbazole derivatives, while those with electron-withdrawing substituents form charge transfer complexes (CTCs) instead of carbazoles. The photoreaction is favored by weak electron-acceptor groups in polar solvents. The absorption and fluorescence spectra of these derivatives show dependence on solvent polarity.

JOURNAL OF ORGANIC CHEMISTRY (2023)

Article Chemistry, Organic

Iodine-Catalyzed Annulation Reaction of Ortho-Formylarylketones with Indoles: A General Strategy for the Synthesis of Indolylbenzo[b]carbazoles

Sundaram Suresh et al.

Summary: The iodine-catalyzed cascade reaction between ortho-formylarylketones and indoles for the synthesis of indolylbenzo-[b]carbazoles is described. The reaction involves two successive nucleophilic additions of indoles to the aldehyde group of ortho-formylarylketones, while the ketone functionality does not participate in the nucleophilic addition and undergoes only Friedel-Crafts-type cyclization. The efficiency of this reaction is demonstrated with gram-scale reactions using various substrates.

JOURNAL OF ORGANIC CHEMISTRY (2023)

Article Chemistry, Organic

Bronsted Acid-Catalyzed Reaction of N-arylnaphthalen-2-amines with Quinone Esters for the Construction of Carbazole and C-N Axially Chiral Carbazole Derivatives

Mingliang Zhang et al.

Summary: We demonstrated an efficient synthetic method for carbazole derivatives using N- arylnaphthalen-2-amines and quinone esters catalyzed by Bronsted acid. The reaction yielded a series of carbazole derivatives in good to excellent yields under mild conditions. Additionally, using chiral phosphoric acid as a catalyst, a series of C-N axially chiral carbazole derivatives were successfully constructed with moderate to excellent atroposelectivities, providing a novel strategy for the atroposelective construction of C-N axially chiral compounds.

JOURNAL OF ORGANIC CHEMISTRY (2023)

Article Chemistry, Multidisciplinary

Synthesis and photophysical properties of fluorescent 8,9-diarylbenzo[def]carbazoles

Huan-Chang Hsiao et al.

Summary: We report the synthesis and photophysical properties of N-acyl and N-free 8,9-diarylbenzo[def]carbazoles. The 8,9-diarylbenzo[def]carbazoles show lower energy levels and smaller HOMO/LUMO gap compared to the parent benzo[def]carbazole, and the N-unprotected ones show more red-shifted fluorescent emission compared to the N-acyl ones. These 8,9-diaryl substituted benzo[def]carbazoles in CHCl3 exhibit absorption and emission maxima in the ranges of 278-350 and 365-426 nm, respectively, with high quantum yields (phi(F)) up to 0.62.

JOURNAL OF THE CHINESE CHEMICAL SOCIETY (2023)

Review Biochemistry & Molecular Biology

Green Synthesis of Aromatic Nitrogen-Containing Heterocycles by Catalytic and Non-Traditional Activation Methods

R. Bernadett Vlocsko et al.

Summary: This review summarizes recent progress in the environmentally friendly synthesis of aromatic N-heterocycles, focusing on the use of catalytic methods and non-traditional activation. The article is divided into two parts: the preparation of single ring N-heterocycles and their condensed analogs. Both categories include compounds with one, two, or multiple N-atoms. Due to the numerous protocols available, the review highlights representative examples to showcase the different methods.

MOLECULES (2023)

Article Chemistry, Organic

Synthesis of Cyclohepta[b]indoles and Furo[3,4-b]carbazoles from Indoles, Tertiary Propargylic Alcohols, and Activated Alkynes

Hailing Yin et al.

Summary: A metal-free and environmentally friendly approach to cyclohepta[b]indole and furo[3,4-b]carbazole frameworks via a three-component reaction from indoles, tertiary propargylic alcohols, and activated alkynes is described. The probable mechanism was proposed based on the isolation and characterization of a key intermediate. Gram-scale reaction and product derivatizations were performed to demonstrate the practicality of the developed methodology.

ORGANIC LETTERS (2023)

Article Chemistry, Organic

Br?nsted-Acid-Catalyzed Friedel-Crafts Reaction and Electrocyclization Cascade of Indoles with ?-Functionalized Carbonyls

Linbo Tan et al.

Summary: An efficient Friedel-Crafts-type reaction followed by electrocyclization cascade has been developed using readily available starting materials, ethanol as a solvent, and Bronsted acid as a catalyst under an air atmosphere. The strategy has been successfully applied to the synthesis of 2-(2-aminophenyl)-9H-carbazole with excellent regioselectivity, functional group tolerance, and scalability. Additionally, the one-pot synthesis of quino[3,4-a]carbazoles has been achieved, demonstrating the broad synthetic utility of this strategy for the synthesis of valuable heteroaryl-annulated [a]carbazoles.

ORGANIC LETTERS (2023)

Review Chemistry, Physical

Review on Carbazole-Based Hole Transporting Materials for Perovskite Solar Cell

Krishnapriya Radhakrishna et al.

Summary: Solar cells made of organic-inorganic metal halide perovskite have the potential to replace traditional silicon-based solar cells, but their efficiency is a major hurdle in commercialization. The use of suitable organic hole transporting materials can improve the efficiency of perovskite solar cells. Spiro-OMeTAD is the standard hole transporting material used, but its complex synthesis and purification steps make it cost-ineffective. Recently, hole transporting materials made of organic small molecules, such as carbazole, have shown better photovoltaic properties and cost-effectiveness. This review focuses on the design and synthesis strategies of carbazole-based hole transporting materials and evaluates their performance in perovskite solar cells.

ACS APPLIED ENERGY MATERIALS (2023)

Article Engineering, Electrical & Electronic

Insight into the Diindolo[3,2-b:2′,3′-h]carbazole Core as an Air-Stable Semiconductor for OTFTs

Roger Bujaldon et al.

Summary: This study presents the synthesis of five diindolo[3,2-b:2 ',3 '-h]carbazole derivatives and their application in organic thin-film transistors. The single-crystal structures of these compounds were elucidated by powder X-ray diffraction analysis, providing insight into the intermolecular arrangement. By fine-tuning the length of alkyl chains and the type of passivation layer, a range of mobility values from 10(-6) to 10(-3) cm(2) V-1 s(-1) was achieved. Remarkably, these devices exhibited excellent temporal and air stability with a shelf lifetime of up to several years, confirming the potential of this research.

ACS APPLIED ELECTRONIC MATERIALS (2023)

Article Chemistry, Organic

Palladium-Catalyzed Double N-Arylation to Access Unsymmetric N,N′-Bicarbazole Scaffolds

Huan Zhang et al.

Summary: Here, the authors report a palladium-catalyzed double C-N coupling reaction between 9H-carbazol-9-amines and 2,2'-dibromo-1,1'-biphenyl. This method provides a route to synthesize N,N'-bicarbazole scaffolds, which are commonly used as linkers in the construction of functional covalent organic frameworks (COFs). The authors successfully synthesized various substituted N,N'-bicarbazoles in moderate to high yields, and demonstrated the potential application of this method in the synthesis of COF monomers like tetrabromide 4 and tetraalkynylate 5.

JOURNAL OF ORGANIC CHEMISTRY (2023)

Article Chemistry, Applied

Gold-Catalyzed Cyclizations and [3+2]-Annulation Cascades between 1,5-Diyn-3-ols and Nitrones to Construct Carbazole Frameworks

Sudhakar Dattatray Tanpure et al.

Summary: Gold-catalyzed cascade reactions between 1,5-diyn-3-ols and nitrones have been developed for the synthesis of carbazole derivatives. This reaction provides a facile approach for the synthesis of polyaromatic compounds containing carbazole subunits. The unexpected oxoarylation reaction, instead of the known oxidative Mannich reaction for but-1-yn-4-ols, is attributed to the presence of a second alkyne in 1,5-diyn-3-ols, which weakens the bonding between gold and this alkyne and restricts the conformational flexibility of the tethered alcohol.

ADVANCED SYNTHESIS & CATALYSIS (2023)

Review Chemistry, Multidisciplinary

[RhCp*Cl-2](2)-Catalyzed Indole Functionalization: Synthesis of Bioinspired Indole-Fused Polycycles

Amar Nath Singh Chauhan et al.

Summary: Polycyclic fused indoles, which are widely found in natural products and pharmaceuticals, have diverse structures and biological relevance, making them suitable for exploring chemical space. Rhodium(III)-catalyzed processes have been developed for the efficient synthesis of these indole-based polycycles, leading to significant progress in the synthesis of biologically active compounds. This review focuses on the recent developments in cascade annulation methods catalyzed by Rh(III) for synthesizing fused indoles, providing insights into synthetic designs and mechanisms. Synthetic methods for polycyclic carbocycles and heterocycles with at least three fused cages are also discussed, including newly created concepts and toolkits.

ACS OMEGA (2023)

Review Polymer Science

Mini-review on the novel synthesis and potential applications of carbazole and its derivatives

Zhichao Xu et al.

Summary: This review systematically reviews the synthesis, characterization, and application of carbazole-based polymers, as well as the relationship between their structures and properties. It highlights the potential of these polymers in greenhouse gas capture and emphasizes the importance of reasonable molecular design and efficient synthesis in obtaining functional polymer materials with high gas capture capacity and selective absorption.

DESIGNED MONOMERS AND POLYMERS (2023)

Review Chemistry, Organic

Triflic Anhydride (Tf2O)-Activated Transformations of Amides, Sulfoxides and Phosphorus Oxides via Nucleophilic Trapping

Hai Huang et al.

Summary: This review discusses the features and applications of trifluoromethanesulfonic anhydride (Tf2O) in organic synthesis, particularly in amide, sulfoxide, and phosphorus oxide chemistry through electrophilic activation. The versatile triflate intermediate generated by Tf2O can react with diverse nucleophiles to yield novel compounds.

SYNTHESIS-STUTTGART (2022)

Article Chemistry, Physical

The Photoinduced Electrocyclization Reaction of Triphenylamine (TPA) in Sustainable and Confined Micellar Solutions: A Steady-State and Laser Flash Photolysis Approach

Rocio A. Sanmartin et al.

Summary: The irradiation of triphenylamine (TPA) under homogeneous and micellar conditions was investigated. The formation rate of N-phenylcarbazole (N-PhCA) was found to be faster in micellar solution due to the confined environment and hydrophobic micellar core. The transient N-phenyl-4a,4b-dihydrocarbazole (DHC0) was detected via laser flash photolysis.

CHEMPHOTOCHEM (2022)

Article Chemistry, Organic

Hydrogen-Borrowing Reduction/Dehydrogenative Aromatization of Nitroarenes through Visible-Light-Induced Energy Transfer: An Entry to Pyrimidoindazoles and Carbazoles

Zhonghua Qu et al.

Summary: In this study, a novel visible-light-induced protocol for hydrogen-borrowing reduction/dehydrogenation aromatization/cyclization of nitroarenes by energy transfer is described. The protocol does not require additional oxidants, hydrogen acceptors, and hydrogen evolution metal catalysts. Mechanistic studies showed that the hydrogen-borrowing reduction/dehydrogenative aromatization process is initiated by the formation of active singlet species through efficient energy transfer of excited Ir[dF(CF3)ppy]2(dtbpy)PF6 to nitroarenes.

ORGANIC LETTERS (2022)

Article Chemistry, Organic

Benzotriazoles and Triazoloquinones: Rearrangements to Carbazoles, Benzazirines, Azepinediones, and Fulvenimines

Jeremy Marchais et al.

Summary: The denitrogenative rearrangements of various benzotriazoles were studied using DFT and CASPT2 calculations, showing different reaction pathways for different types of benzotriazoles during pyrolysis or photolysis.

JOURNAL OF ORGANIC CHEMISTRY (2021)

Article Chemistry, Multidisciplinary

Visible-light-driven Cadogan reaction

Zhonghua Qu et al.

Summary: A visible-light-driven photochemical Cadogan-type cyclization has been discovered, utilizing the organic D-A type photosensitizer 4CzIPN to efficiently transfer energy and enable access to carbazoles and related heterocycles. Experimental and DFT calculation results demonstrate the robust synthetic capacity and good tolerance of various functionalities in this reaction system.

CHINESE CHEMICAL LETTERS (2021)

Article Biochemistry & Molecular Biology

Photochemistry of Tris(2,4-dibromophenyl)amine and its Application to Co-oxidation on Sulfides and Phosphines

Sergio M. Bonesi et al.

Summary: The photochemistry of tris(2,4-dibromophenyl)amine was studied using time-resolved nanosecond spectroscopy, revealing the formation of N-aryl-4a,4b-dihydrocarbazole radical cation and hydroperoxyl radical through intermediate Magic Green. Additionally, the photogenerated Magic Green was found to promote the co-oxidation of nucleophilic triarylphosphines to triarylphosphine oxides while preventing amine cyclization, with the Ar3POO·+ intermediate playing a key role in phosphine oxide formation.

PHOTOCHEMISTRY AND PHOTOBIOLOGY (2021)

Article Chemistry, Multidisciplinary

Electrochemical Dehydrogenative C(sp2)-H Amination

Mahesh Puthanveedu et al.

Summary: A transition-metal-free direct electrolytic C-H amination involving an electrochemically generated nitrenium ion intermediate has been developed. The electrosynthesis takes place in the absence of any organoiodine catalysts and is enabled by an in situ generated electrolyte. A novel, efficient intramolecular and intermolecular C-H amination has been demonstrated using a simple reaction setup.

CHEMISTRY-A EUROPEAN JOURNAL (2021)

Article Chemistry, Multidisciplinary

Photochemistry of triphenylamine (TPA) in homogeneous solution and the role of transient N-phenyl-4a,4b-dihydrocarbazole. A steady-state and time-resolved investigation

Stefano Protti et al.

Summary: The photoreactivity of triphenylamine in homogeneous media was investigated using laser flash photolysis spectroscopy and preparative experiments to evaluate the photophysical and photochemical behavior of transient N-phenyl-4a,4b-dihydrocarbazole (DHC0) under polar and non-polar solvents. The kinetic parameters of DHC0, including lifetime and rate constants, were measured, and its intermediacy in the co-oxidation of nucleophilic substrates was studied. Two oxidizing intermediates were formed from DHC0 in the presence of molecular oxygen, with different reactions on triarylphosphines and sulfides.

NEW JOURNAL OF CHEMISTRY (2021)

Article Chemistry, Organic

Site-Specific Synthesis of Carbazole Derivatives through Aryl Homocoupling and Amination

Jaeyoung Ban et al.

SYNTHESIS-STUTTGART (2020)

Article Chemistry, Organic

Synthesis of Benzocarbazole Derivatives by Photocyclization

Valeriya G. Melekhina et al.

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2019)

Article Chemistry, Organic

Photorearrangement of dihetarylethenes as a tool for the benzannulation of heterocycles

Andrey G. Lvov et al.

ORGANIC & BIOMOLECULAR CHEMISTRY (2019)

Article Chemistry, Multidisciplinary

Visible-light-promoted intramolecular C-H amination in aqueous solution: synthesis of carbazoles

Lizheng Yang et al.

GREEN CHEMISTRY (2018)

Article Chemistry, Organic

Photochemical Co-Oxidation of Sulfides and Phosphines with Tris(p-bromophenyl)amine. A Mechanistic Study

Sergio M. Bonesi et al.

JOURNAL OF ORGANIC CHEMISTRY (2018)

Article Chemistry, Multidisciplinary

Photochemical intramolecular amination for the synthesis of heterocycles

Shawn Parisien-Collette et al.

GREEN CHEMISTRY (2017)

Article Chemistry, Multidisciplinary

Titanium dioxide visible light photocatalysis: surface association enables photocatalysis with visible light irradiation

Spencer P. Pitre et al.

CHEMICAL COMMUNICATIONS (2017)

Review Chemistry, Multidisciplinary

Flash Vacuum Pyrolysis of Azides, Triazoles, and Tetrazoles

Curt Wentrup

CHEMICAL REVIEWS (2017)

Review Chemistry, Multidisciplinary

Heteroleptic Cu-Based Sensitizers in Photoredox Catalysis

Augusto C. Hernandez-Perez et al.

ACCOUNTS OF CHEMICAL RESEARCH (2016)

Article Chemistry, Organic

Synthesis of the Carbazole Scaffold Directly from 2-Aminobiphenyl by Means of Tandem C-H Activation and C-N Bond Formation

Hans-Rene Bjorsvik et al.

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2016)

Article Chemistry, Organic

Palladium-Catalyzed Intramolecular C-H Amination in Water

Lizheng Yang et al.

EUROPEAN JOURNAL OF ORGANIC CHEMISTRY (2016)

Article Chemistry, Multidisciplinary

Photochemical Synthesis of Complex Carbazoles: Evaluation of Electronic Effects in Both UV- and Visible-Light Methods in Continuous Flow

Augusto C. Hernandez-Perez et al.

CHEMISTRY-A EUROPEAN JOURNAL (2015)

Article Chemistry, Multidisciplinary

Photoinduced Macroscopic Morphological Transformation of an Amphiphilic Diarylethene Assembly: Reversible Dynamic Motion

Kenji Higashiguchi et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2015)

Review Chemistry, Multidisciplinary

Photochromism of Diarylethene Molecules and Crystals: Memories, Switches, and Actuators

Masahiro Irie et al.

CHEMICAL REVIEWS (2014)

Article Chemistry, Organic

Synthesis of Carbazoles by Copper-Catalyzed Intramolecular C-H/N-H Coupling

Kazutaka Takamatsu et al.

ORGANIC LETTERS (2014)

Article Chemistry, Applied

Synthesis of a Carprofen Analogue Using a Continuous Flow UV-Reactor

Antoine Caron et al.

ORGANIC PROCESS RESEARCH & DEVELOPMENT (2014)

Article Chemistry, Organic

(Co)oxidation/cyclization processes upon irradiation of triphenylamine

Sergio Mauricio Bonesi et al.

TETRAHEDRON LETTERS (2014)

Article Chemistry, Multidisciplinary

A Visible-Light-Mediated Synthesis of Carbazoles

Augusto C. Hernandez-Perez et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2013)

Review Chemistry, Multidisciplinary

Amino-Directed RhIII-Catalyzed CH Activation Leading to One-Pot Synthesis of NH Carbazoles

Qibai Jiang et al.

CHEMISTRY-A EUROPEAN JOURNAL (2013)

Review Chemistry, Organic

Synthesis of Pyrroles, Indoles, and Carbazoles through Transition-Metal-Catalyzed C-H Functionalization

Naohiko Yoshikai et al.

ASIAN JOURNAL OF ORGANIC CHEMISTRY (2013)

Review Chemistry, Multidisciplinary

Occurrence, Biogenesis, and Synthesis of Biologically Active Carbazole Alkaloids

Arndt W. Schmidt et al.

CHEMICAL REVIEWS (2012)

Article Chemistry, Physical

Electrochemically Induced Reversible and Irreversible Coupling of Triarylamines

Olena Yurchenko et al.

JOURNAL OF PHYSICAL CHEMISTRY B (2012)

Article Chemistry, Multidisciplinary

Synthesis and Physical Properties of Four Hexazapentacene Derivatives

Gang Li et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2012)

Article Chemistry, Organic

Recent trends in the synthesis of carbazoles: an update

Joyeeta Roy et al.

TETRAHEDRON (2012)

Article Materials Science, Multidisciplinary

Organic light-emitting devices fabricated utilizing core/shell CdSe/ZnS quantum dots embedded in a polyvinylcarbazole

Kwang Seop Lee et al.

JOURNAL OF MATERIALS SCIENCE (2011)

Article Chemistry, Multidisciplinary

Concise Palladium-Catalyzed Synthesis of Dibenzodiazepines and Structural Analogues

Dmitry Tsvelikhoysky et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2011)

Article Chemistry, Organic

Synthetic Studies on Indolocarbazoles: Total Synthesis of Staurosporine Aglycon

Ganesan Gobi Rajeshwaran et al.

ORGANIC LETTERS (2011)

Article Chemistry, Organic

Synthesis of Active Metabolites of Carvedilol, an Antihypertensive Drug

N. Senthilkumar et al.

SYNTHETIC COMMUNICATIONS (2011)

Article Materials Science, Multidisciplinary

D-π-A organic dyes with carbazole as donor for dye-sensitized solar cells

Kola Srinivas et al.

SYNTHETIC METALS (2011)

Article Chemistry, Multidisciplinary

High and Balanced Hole and Electron Mobilities from Ambipolar Thin-Film Transistors Based on Nitrogen-Containing Oligoacences

Yi-Yang Liu et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2010)

Review Biochemistry & Molecular Biology

Photochemical Oxidative Cyclisation of Stilbenes and Stilbenoids-The Mallory-Reaction

Kare B. Jorgensen

MOLECULES (2010)

Article Chemistry, Organic

Synthesis and biological evaluation of novel benzoxazinic analogues of ellipticine

Deborah Mousset et al.

TETRAHEDRON LETTERS (2010)

Article Chemistry, Organic

Photophysical Study of Blue, Green, and Orange-Red Light-Emitting Carbazoles

Ravi M. Adhikari et al.

JOURNAL OF ORGANIC CHEMISTRY (2009)

Article Chemistry, Multidisciplinary

Toward a rational design of poly(2,7-carbazole) derivatives for solar cells

Nicolas Blouin et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2008)

Article Materials Science, Multidisciplinary

Well-defined [3,3 ']bicarbazolyl-based electroactive compounds for optoelectronics

V. Vaitkeviciene et al.

SYNTHETIC METALS (2008)

Article Chemistry, Physical

Indolyl-substituted carbazole derivatives as amorphous electro-active materials for optoelectronics

V. Peciuraite et al.

JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY (2006)

Article Chemistry, Multidisciplinary

Multifunctional iridium complexes based on carbazole modules as highly efficient electrophosphors

Wai-Yeung Wong et al.

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION (2006)

Review Biochemistry & Molecular Biology

Indolocarbazole natural products: occurrence, biosynthesis, and biological activity

Cesar Sanchez et al.

NATURAL PRODUCT REPORTS (2006)

Article Chemistry, Physical

Well defined carbazol-3,9-diyl based oligomers with diphenylamino end-cap as novel amorphous molecular materials for optoelectronics

S Grigalevicius et al.

JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY (2005)

Review Polymer Science

Polycarbazoles:: 25 years of progress

JF Morin et al.

MACROMOLECULAR RAPID COMMUNICATIONS (2005)

Article Chemistry, Organic

Synthesis of carbazomycin B by radical arylation of benzene

D Crich et al.

TETRAHEDRON (2004)

Article Chemistry, Organic

1,8-diamino-3,6-dichlorocarbazole: A promising building block for anion receptors

MJ Chmielewski et al.

ORGANIC LETTERS (2004)

Review Polymer Science

Carbazole-containing polymers: synthesis, properties and applications

JV Grazulevicius et al.

PROGRESS IN POLYMER SCIENCE (2003)

Review Chemistry, Multidisciplinary

Isolation and synthesis of biologically active carbazole alkaloids

HJ Knölker et al.

CHEMICAL REVIEWS (2002)

Article Chemistry, Multidisciplinary

Simple Cu(I) complexes with unprecedented excited-state lifetimes

DG Cuttell et al.

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY (2002)

Article Chemistry, Multidisciplinary

Novel photoreaction of N-alkyl(p-methoxyphenyl) arylamines assisted by protic acids

JH Ho et al.

CHEMICAL COMMUNICATIONS (2002)

Article Chemistry, Medicinal

The first synthesis of clausenamine-A and cytotoxic activities of three biscarbazole analogues against cancer cells

AM Zhang et al.

BIOORGANIC & MEDICINAL CHEMISTRY LETTERS (2000)