C–H functionalization of azines. Anodic dehydroaromatization of 9-(hetero)aryl-9,10-dihydroacridines

A. V. Shchepochkin, O. N. Chupakhin, V. N. Charushin, D. V. Steglenko, V. I. Minkin, G. L. Rusinov and A. I. Matern

RSC Adv., 2016, 6, 77834
DOI: 10.1039/C6RA17783B

A magnetic nanoparticle-supported N-heterocyclic carbene-palladacycle: an efficient and recyclable solid molecular catalyst for Suzuki–Miyaura cross-coupling of 9-chloroacridine

Qinyue Deng, Yajing Shen, Haibo Zhu and Tao Tu

Chem. Commun., 2017, 53, 13063
DOI: 10.1039/C7CC06958H

Palladium(II)-Catalyzed Oxidative C–H/C–H Coupling and Eliminative SNH Reactions in Direct Functionalization of Imidazole Oxides with Indoles

Mikhail V. Varaksin, Irina A. Utepova, Oleg N. Chupakhin and Valery N. Charushin

J. Org. Chem., 2012, 77, 9087
DOI: 10.1021/jo301618b

Electrochemical Oxidative Aromatizationof 9-Substituted 9,10-Dihydroacridines: Cleavage of C–H vs C–X Bond

Oleg N. Chupakhin, Alexander V. Shchepochkin, Valery N. Charushin, Anna V. Maiorova, Tatyana V. Kulikova, Konstantin Yu. Shunyaev, Andrey N. Enyashin, Pavel A. Slepukhin and Anna I. Suvorova

Chem Heterocycl Comp, 2019, 55, 956
DOI: 10.1007/s10593-019-02562-x

2-Aminobenzaldehyde, a common precursor to acridines and acridones endowed with bioactivities

Sarah Zeghada, Ghenia Bentabed-Ababsa, Olivier Mongin, William Erb, Laurent Picot, Valérie Thiéry, Thierry Roisnel, Vincent Dorcet and Florence Mongin

Tetrahedron, 2020, 76, 131435
DOI: 10.1016/j.tet.2020.131435

Modular Assembly of Acridines by Integrating Photo‐Excitation of o‐Alkyl Nitroarenes with Copper‐Promoted Cascade Annulation

Haichao Huang, Yifan Jiang, Wei Yuan and Yu‐Mei Lin

Angew Chem Int Ed, 2024
DOI: 10.1002/anie.202409653

Nickel-Catalyzed Direct Alkylation of C–H Bonds in Benzamides and Acrylamides with Functionalized Alkyl Halides via Bidentate-Chelation Assistance

Yoshinori Aihara and Naoto Chatani

J. Am. Chem. Soc., 2013, 135, 5308
DOI: 10.1021/ja401344e

Synthesis of Acridines through Alkyne Addition to Diarylamines

Kristen E. Berger, Grant M. McCormick, Joseph A. Jaye, Christina M. Rozeske and Eric H. Fort

Molecules, 2018, 23, 2867
DOI: 10.3390/molecules23112867

Facile Synthesis of Unsymmetrical Acridines and Phenazines by a Rh(III)-Catalyzed Amination/Cyclization/Aromatization Cascade

Yajing Lian, Joshua R. Hummel, Robert G. Bergman and Jonathan A. Ellman

J. Am. Chem. Soc., 2013, 135, 12548
DOI: 10.1021/ja406131a

Recent Progress in Nickel‐Catalyzed Biaryl Coupling

Junichiro Yamaguchi, Kei Muto and Kenichiro Itami

Eur J Org Chem, 2013, 2013, 19
DOI: 10.1002/ejoc.201200914

Aerobic Transition‐Metal‐Free Synthesis of 2,3‐Diarylindoles and 5‐Aryluracils via Oxidative Nucleophilic Substitution of Hydrogen Pathway

Jin Yu, Hye Ran Moon, Su Yeon Kim and Jae Nyoung Kim

Bulletin Korean Chem Soc, 2016, 37, 112
DOI: 10.1002/bkcs.10629

Isolation, Structure, and Reactivity of an Arylnickel(II) Pivalate Complex in Catalytic C–H/C–O Biaryl Coupling

Kei Muto, Junichiro Yamaguchi, Aiwen Lei and Kenichiro Itami

J. Am. Chem. Soc., 2013, 135, 16384
DOI: 10.1021/ja409803x

Cobalt‐Catalyzed C4‐Selective Direct Alkylation of Pyridines

Takashi Andou, Yutaka Saga, Hirotomo Komai, Shigeki Matsunaga and Motomu Kanai

Angew Chem Int Ed, 2013, 52, 3213
DOI: 10.1002/anie.201208666

Nickel-Catalyzed Site-Selective Alkylation of Unactivated C(sp3)–H Bonds

Xuesong Wu, Yan Zhao and Haibo Ge

J. Am. Chem. Soc., 2014, 136, 1789
DOI: 10.1021/ja413131m

Catalytic Arylation of a CH Bond in Pyridine and Related Six‐Membered N‐Heteroarenes Using Organozinc Reagents

Isao Hyodo, Mamoru Tobisu and Naoto Chatani

Chemistry An Asian Journal, 2012, 7, 1357
DOI: 10.1002/asia.201100971

Alkali-Metal-Mediated Synergistic Effects in Polar Main Group Organometallic Chemistry

Stuart D. Robertson, Marina Uzelac and Robert E. Mulvey

Chem. Rev., 2019, 119, 8332
DOI: 10.1021/acs.chemrev.9b00047

Isolation and identification of the pre-catalyst in iron-catalyzed direct arylation of pyrrole with phenylboronic acid

Samantha M. Brewer, Philip M. Palacios, Hannah M. Johnston, Brad S. Pierce and Kayla N. Green

Inorganica Chimica Acta, 2018, 478, 139
DOI: 10.1016/j.ica.2018.03.036

Palladium‐Catalyzed Regioselective Oxidative Annulation of Cyclohexanones and 2‐Aminophenyl Ketones Using Molecular Oxygen as the Sole Oxidant

Wan‐Lu Mu, Meirong Wang, Hui‐Jing Li, Deng‐Ming Huang, Yi‐Yun Zhang, Chao‐Yi Li, Ying Liu and Yan‐Chao Wu

Adv Synth Catal, 2017, 359, 4250
DOI: 10.1002/adsc.201700715

Total Syntheses of Menisporphine and Daurioxoisoporphine C Enabled by Photoredox-Catalyzed Direct C–H Arylation of Isoquinoline with Aryldiazonium Salt

Jing Zhang, Jie Chen, Xiaoyun Zhang and Xiaoguang Lei

J. Org. Chem., 2014, 79, 10682
DOI: 10.1021/jo5020432

ChemInform Abstract: Regioselective C—H Bond Functionalizations of Acridines Using Organozinc Reagents.

Isao Hyodo, Mamoru Tobisu and Naoto Chatani

ChemInform, 2012, 43
DOI: 10.1002/chin.201218173

The Reduction of Carbonyl Compounds with Dicyclopentylzinc: A New Example of Asymmetric Amplifying Autocatalysis

Elena Sh. Saigitbatalova, Liliya Z. Latypova, Almaz A. Zagidullin, Almira R. Kurbangalieva and Ilya D. Gridnev

IJMS, 2023, 24, 17048
DOI: 10.3390/ijms242317048

Synthesis of Substituted Acridines through a Palladium‐Catalyzed Condensation/Cyclization/Tautomerization Sequence

Xiangui Chen, Yanjun Xie, Cheng Li, Fuhong Xiao and Guo‐Jun Deng

Eur J Org Chem, 2017, 2017, 577
DOI: 10.1002/ejoc.201601553

The Mechanism of NO Bond Cleavage in Rhodium‐Catalyzed CH Bond Functionalization of Quinoline N‐oxides with Alkynes: A Computational Study

Yingzi Li, Song Liu, Zisong Qi, Xiaotian Qi, Xingwei Li and Yu Lan

Chemistry A European J, 2015, 21, 10131
DOI: 10.1002/chem.201500290

tert-Butyl Bromide-Promoted Intramolecular Cyclization of 2-Arylamino Phenyl Ketones and Its Combination with Cu-Catalyzed C–N Coupling: Synthesis of Acridines at Room Temperature

Zifeng Cao, Yuan Zhu, Xiaoman Li, Yang He, Jinli Zhang, Liang Xu and Yu Wei

J. Org. Chem., 2020, 85, 10167
DOI: 10.1021/acs.joc.0c00137

Zincate-Mediated Arylation Reactions of Acridine: Pre- and Postarylation Structural Insights

Alberto Hernán-Gómez, Emma Herd, Marina Uzelac, Thomas Cadenbach, Alan R. Kennedy, Ivana Borilovic, Guillem Aromı́ and Eva Hevia

Organometallics, 2015, 34, 2614
DOI: 10.1021/om501251q

DFT Studies on the Mechanism of Palladium(IV)-Mediated C–H Activation Reactions: Oxidant Effect and Regioselectivity

Yan-Mei Xing, Lei Zhang and De-Cai Fang

Organometallics, 2015, 34, 770
DOI: 10.1021/om501239n

Nickel-Catalyzed Aromatic C–H Functionalization

Junichiro Yamaguchi, Kei Muto and Kenichiro Itami

Top Curr Chem (Z), 2016, 374
DOI: 10.1007/s41061-016-0053-z

Nickel promoted switchable hydroheteroarylation of cyclodienes via C–H bond activation of heteroarenes

Wei-Chih Lee, Wei-Chin Shih, Ting-Hsuan Wang, Yuhua Liu, Glenn P.A. Yap and Tiow-Gan Ong

Tetrahedron, 2015, 71, 4460
DOI: 10.1016/j.tet.2015.03.066

3d Transition Metals for C–H Activation

Parthasarathy Gandeepan, Thomas Müller, Daniel Zell, Gianpiero Cera, Svenja Warratz and Lutz Ackermann

Chem. Rev., 2019, 119, 2192
DOI: 10.1021/acs.chemrev.8b00507

Nickel‐Catalyzed Site‐Selective Amidation of Unactivated C(sp3)H Bonds

Xuesong Wu, Yan Zhao and Haibo Ge

Chemistry A European J, 2014, 20, 9530
DOI: 10.1002/chem.201403356

Modular Assembly of Acridines by Integrating Photo‐Excitation of o‐Alkyl Nitroarenes with Copper‐Promoted Cascade Annulation

Haichao Huang, Yifan Jiang, Wei Yuan and Yu‐Mei Lin

Angewandte Chemie, 2024, 136
DOI: 10.1002/ange.202409653

Decarbonylative C–H Coupling of Azoles and Aryl Esters: Unprecedented Nickel Catalysis and Application to the Synthesis of Muscoride A

Kazuma Amaike, Kei Muto, Junichiro Yamaguchi and Kenichiro Itami

J. Am. Chem. Soc., 2012, 134, 13573
DOI: 10.1021/ja306062c

Cobalt‐Catalyzed C4‐Selective Direct Alkylation of Pyridines

Takashi Andou, Yutaka Saga, Hirotomo Komai, Shigeki Matsunaga and Motomu Kanai

Angewandte Chemie, 2013, 125, 3295
DOI: 10.1002/ange.201208666

C–H Functionalization of Azines

Kei Murakami, Shuya Yamada, Takeshi Kaneda and Kenichiro Itami

Chem. Rev., 2017, 117, 9302
DOI: 10.1021/acs.chemrev.7b00021