Shuddhodan N. Kadam, Ajay N. Ambhore, Rahul D. Kamble, Mahesh G. Wakhradkar, Priya D. Gavhane, Milind V. Gaikwad, Krishna Chaitanya Gunturu and Bhaskar S. Dawane

New J. Chem., 2021, 45, 4632
DOI: 10.1039/D0NJ05904H

Visible-light-promoted selective C–H amination of heteroarenes with heteroaromatic amines under metal-free conditions

Supravat Samanta, Chitrakar Ravi, Sadu Nageswara Rao, Abhisek Joshi and Subbarayappa Adimurthy

Org. Biomol. Chem., 2017, 15, 9590
DOI: 10.1039/C7OB02504A

Metal-free synthesis of 3-methylthiofurans from homopropargylic alcohols and DMSO via a tandem sulfenylation/cyclization reaction in a one-pot manner

Zhenyu An, Yue She, Xiaodong Yang, Xiaobo Pang and Rulong Yan

Org. Chem. Front., 2016, 3, 1746
DOI: 10.1039/C6QO00462H

HFIP promoted thio(hetero)arylation of imidazoheterocycles under metal- and base-free conditions

Narendra R. Chaubey and Anant R. Kapdi

Chem. Commun., 2021, 57, 8202
DOI: 10.1039/D1CC03089B

Synthesis of thiophosphates through a three-component reaction by using sulfur dioxide as the sulfur source

Xinxing Gong, Jiahao Chen, Jianhe Liu and Jie Wu

Org. Chem. Front., 2017, 4, 2221
DOI: 10.1039/C7QO00634A

Copper-catalyzed chalcogenation of imidazoheterocycles with sulfur/selenium powder and coumarinyl triflates

Tao Guo, Xu-Ning Wei, Hong-Yan Wang, Ying-Li Zhu, Yun-Hui Zhao and Yong-Cheng Ma

Org. Biomol. Chem., 2017, 15, 9455
DOI: 10.1039/C7OB02278F

Three-component difunctionalization of alkenes leading to β-acetamido sulfides and β-acetoxy sulfides

Dingyi Wang, Zhaohua Yan, Qihuang Xie, Rongxing Zhang, Sen Lin and Yuanxing Wang

Org. Biomol. Chem., 2017, 15, 1998
DOI: 10.1039/C7OB00110J

Indium-based metal–organic frameworks as catalysts: synthesis of 2-nitro-3-arylimidazo[1,2-a]pyridines via oxidative amination under air using MIL-68(In) as an effective heterogeneous catalyst

Phuong T. M. Ha, Thien N. Lieu, Son H. Doan, Trang T. B. Phan, Tung T. Nguyen, Thanh Truong and Nam T. S. Phan

RSC Adv., 2017, 7, 23073
DOI: 10.1039/C7RA02802D

Electrochemical C3-methylthiolation of imidazopyridines with dimethyl sulfoxide

Zhaoyue Feng, Yingsibing Fan, Congcong Qiang, Ping Liu and Peipei Sun

Green Chem., 2024, 26, 3517
DOI: 10.1039/D4GC00314D

Three-component oxysulfenylation reaction: two simple and convenient approaches to β-alkoxy sulfides

Dingyi Wang, Rongxing Zhang, Wei Ning, Zhaohua Yan and Sen Lin

Org. Biomol. Chem., 2016, 14, 5136
DOI: 10.1039/C6OB00646A

Iodine-catalyzed direct C–H thiolation of imidazo[1,5-a]quinolines for the synthesis of 3-sulfenylimidazo[1,5-a]quinolines

Song-Song Wu, Cheng-Tao Feng, Di Hu, Ye-Kai Huang, Zhong Li, Zai-Gang Luo and Shi-Tang Ma

Org. Biomol. Chem., 2017, 15, 1680
DOI: 10.1039/C6OB02736A

Iodine(iii)-promoted oxidative carbotrifluoromethylation of maleimides with imidazopyridines and Langlois’ reagent

Dipti Lai, Suvam Bhattacharjee, Saurodeep Mandal, Sumit Ghosh, Prithidipa Sahoo, Subrata Sinha and Alakananda Hajra

Chem. Commun., 2024, 60, 2232
DOI: 10.1039/D3CC05889A

Cu-catalyzed sulfenylation of imidazol[1,2-a]pyridine via C–H functionalization using a combination of Na2S2O3 and halides

Yingcai Ding, Ping Xie, Wenhui Zhu, Baojun Xu, Wannian Zhao and Aihua Zhou

RSC Adv., 2016, 6, 81932
DOI: 10.1039/C6RA18136H

Visible light-induced C–H sulfenylation using sulfinic acids

Pengfei Sun, Daoshan Yang, Wei Wei, Min Jiang, Zuli Wang, Liyan Zhang, Hui Zhang, Zhenzhen Zhang, Yu Wang and Hua Wang

Green Chem., 2017, 19, 4785
DOI: 10.1039/C7GC01891F

Magnetically recoverable catalysts for efficient multicomponent synthesis of organosulfur compounds

Fadhil Faez Sead, Vicky Jain, Anjan Kumar, Rekha M. M., Mayank Kundlas, Sofia Gupta, Mukesh Kumari, Mosstafa Kazemi and Ramin Javahershenas

RSC Adv., 2025, 15, 3928
DOI: 10.1039/D4RA08769K

Annulation of imidazo[1,2-a]pyridines under metal-free conditions

Rashmi Semwal, Abhisek Joshi, Rahul Kumar and Subbarayappa Adimurthy

New J. Chem., 2020, 44, 20530
DOI: 10.1039/D0NJ04521G

Visible light-driven, persulfate-mediated dual C–H sulfenylation of imidazopyridines using thiocyanate salt

Pallavi Saha, Vijay Kumar and Deepak K Sharma

New J. Chem., 2024, 48, 18651
DOI: 10.1039/D4NJ03694H

An Efficient Sequential One‐Pot Approach for the Synthesis of C3‐Functionalized Imidazo[1,2‐a]pyridines under Transition‐Metal Free Conditions

Raju Jannapu Reddy, Angothu Shankar and Arram Haritha Kumari

Asian J Org Chem, 2019, 8, 2269
DOI: 10.1002/ajoc.201900606

DMSO/SOCl2-Enabled Synthesis of 3-Chloroindoles via Desulfonylative Chlorocyclization of N,N-Disubstituted 2-Alkynylanilines

Xuemin Li, Yifu Cheng, Yue Li, Fengxia Sun, Xiangyu Zhan, Zhifang Yang, Jingyue Yang and Yunfei Du

J. Org. Chem., 2024, 89, 2039
DOI: 10.1021/acs.joc.3c02471

Sulfonyl hydrazide induced sulfenylation of imidazoheteroarenes: A ‘catalyst and solvent free’ protocol

Sourav Mal and Manoranjan Jana

Synthetic Communications, 2022, 52, 1059
DOI: 10.1080/00397911.2022.2069506

KI/K2S2O8‐Mediated C‐S/C‐N Bond Formation: One‐Pot Regioselective Synthesis of 5H‐Thiazolo[3,2‐a]pyrimidines

Zan Yang, Si Liu, An Li, Jiashu Liao, Lijun Li, Tao Yang and Congshan Zhou

ChemistrySelect, 2019, 4, 6583
DOI: 10.1002/slct.201900793

NH4I-catalyzed chalcogen(S/Se)-functionalization of 5-membered N-heteroaryls under metal-free conditions

Luana Bettanin, Sumbal Saba, Carlos V. Doerner, Marcelo S. Franco, Marcelo Godoi, Jamal Rafique and Antonio L. Braga

Tetrahedron, 2018, 74, 3971
DOI: 10.1016/j.tet.2018.05.084

KOH-mediated intramolecular amidation and sulfenylation: A direct approach to access 3-(arylthio)imidazo[1,2-a]pyridin-2-ols

Khima Pandey, Vikki N. Shinde, Krishnan Rangan and Anil Kumar

Tetrahedron, 2020, 76, 131499
DOI: 10.1016/j.tet.2020.131499

C3 Sulfenylation of N‐Heteroarenes in Water under Catalyst‐Free Conditions

Chitrakar Ravi, Abhisek Joshi and Subbarayappa Adimurthy

Eur J Org Chem, 2017, 2017, 3646
DOI: 10.1002/ejoc.201700487

Synthesis of Imidazo[1,2‐a]pyridines: C‐H Functionalization in the Direction of C‐S Bond Formation

Chitrakar Ravi and Subbarayappa Adimurthy

The Chemical Record, 2017, 17, 1019
DOI: 10.1002/tcr.201600146

Synthesis of 3-methylthioimidazo[1,2-a]pyridines derivatives

Chemical Data Collections, 2021, 31, 100632
DOI: 10.1016/j.cdc.2020.100632

Base‐Promoted Substitution Reaction: A Simple, Economical, and Efficient Method for Obtaining 3‐Sulfenylated Benzo[b]furan Derivatives

Cong Wang, Yuxin Fan, Yaoyao Yao, Wenzhang Chen, Xing Cui, Gaofeng Zhu, Wei Zhou and Lei Tang

ChemistrySelect, 2018, 3, 29
DOI: 10.1002/slct.201702142

Organophosphorus‐Catalyzed Deoxygenation of Sulfonyl Chlorides: Electrophilic (Fluoroalkyl)sulfenylation by PIII/PV=O Redox Cycling

Avipsa Ghosh, Morgan Lecomte, Shin‐Ho Kim‐Lee and Alexander T. Radosevich

Angew Chem Int Ed, 2019, 58, 2864
DOI: 10.1002/anie.201813919

Rhodium catalyzed direct C3-ethoxycarbonylmethylation of imidazo[1,2-a]pyridines with ethyl diazoacetate

Qiuyao Huang, Hui Dong, Bingbing Li, Wenhao Hu and Yuanxiang Wang

Tetrahedron, 2020, 76, 130998
DOI: 10.1016/j.tet.2020.130998

Synthesis of Aryl Methyl Sulfides from Arysulfonyl Chlorides with Dimethyl Carbonate as the Solvent and C1 Source

Ren‐Guan Miao, Xinxin Qi and Xiao‐Feng Wu

Eur J Org Chem, 2021, 2021, 5219
DOI: 10.1002/ejoc.202101037

Catalyst‐free Azo‐arylation of Arenes/Heteroarenes at Room Temperature

Rahul Kumar, Chitrakar Ravi, Abhisek Joshi, Rashmi Semwal and Subbarayappa Adimurthy

ChemistrySelect, 2019, 4, 5740
DOI: 10.1002/slct.201901308

Metal‐Free Four‐Component Strategy to Access Thioether‐Derived Imidazo[1,2‐a]pyridines and Imidazo[2,1‐b]thiazoles

Arram Haritha Kumari, Shreya Ghosh, Naveena S. Veeranagaiah, Raghavaiah Pallepogu and Raju Jannapu Reddy

Eur J Org Chem, 2025
DOI: 10.1002/ejoc.202500394

Crystal Correlation Of Heterocyclic Imidazo[1,2-a]pyridine Analogues and Their Anticholinesterase Potential Evaluation

Huey Chong Kwong, C. S. Chidan Kumar, Siau Hui Mah, Yew Leng Mah, Tze Shyang Chia, Ching Kheng Quah, Gin Keat Lim and Siddegowda Chandraju

Sci Rep, 2019, 9
DOI: 10.1038/s41598-018-37486-7

Iodine-Mediated Difunctionalization of Imidazopyridines with Sodium Sulfinates: Synthesis of Sulfones and Sulfides

Yu-Jing Guo, Shuai Lu, Lu-Lu Tian, En-Ling Huang, Xin-Qi Hao, Xinju Zhu, Tian Shao and Mao-Ping Song

J. Org. Chem., 2018, 83, 338
DOI: 10.1021/acs.joc.7b02734

Base‐Promoted Transition‐Metal‐Free Arylation of Imidazo‐Fused Heterocycles with Diaryliodonium Salts

Rahul Kumar, Chitrakar Ravi, Deepa Rawat and Subbarayappa Adimurthy

Eur J Org Chem, 2018, 2018, 1665
DOI: 10.1002/ejoc.201800286

Iodine-Catalyzed Cross Dehydrogenative Coupling Reaction: A Regioselective Sulfenylation of Imidazoheterocycles Using Dimethyl Sulfoxide as an Oxidant

Yogesh Siddaraju and Kandikere Ramaiah Prabhu

J. Org. Chem., 2016, 81, 7838
DOI: 10.1021/acs.joc.6b01487

Aryl sulfonyl chlorides and sodium aryl sulfinates: non-volatile, non-stench, and non-toxic aryl thiol surrogates for direct aryl-sulfenylation of C–H bonds

Xiaohui Lu, Qicheng Yi, Xicai Pan, Peifang Wang and Esmail Vessally

Journal of Sulfur Chemistry, 2020, 41, 210
DOI: 10.1080/17415993.2019.1683181

t-BuOK-promoted methylthiolation of aryl fluorides with dimethyldisulfide under transition-metal-free and mild conditions

Dayun Huang and Xiangmei Wu

Journal of Fluorine Chemistry, 2021, 245, 109778
DOI: 10.1016/j.jfluchem.2021.109778

PPh3‐Mediated Nucleophilic Sulfonation of Sulfonyl Chlorides with Arynes: Access to Manifold Aryl Sulfones

Hui‐Qi Yue, Qi‐Wei Li, Da‐Wei Shi, Rui‐Jia Yang, Liang‐Liang Han and Bin Yang

Eur J Org Chem, 2023, 26
DOI: 10.1002/ejoc.202300812

Copper-catalyzed three-component reaction of imidazo[1,2-a]pyridine with elemental sulfur and arylboronic acid to produce sulfenylimidazo[1,2-a]pyridines

Genhua Xiao, Hao Min, Zhilei Zheng, Guobo Deng and Yun Liang

Chinese Chemical Letters, 2018, 29, 1363
DOI: 10.1016/j.cclet.2017.12.013

Visible Light‐Induced Energy Transfer Mediated Regioselective C‐3 Thiolation of Imidazoheterocycles using Bunte Salts

Sehdev Kumar, Anoop Sharma, Raman Kumar and Anuj Sharma

Chemistry An Asian Journal, 2025, 20
DOI: 10.1002/asia.202401875

A Facile Synthesis of 3‐(Arylthio)imidazo[1,2‐a]pyridin‐2(3H)‐ones from 2‐Aminopyridinium Bromides and Sodium Arenesulfinates

Saroj, Krishnan Rangan and Anil Kumar

Eur J Org Chem, 2020, 2020, 7015
DOI: 10.1002/ejoc.202000996

Metal‐, Oxidant‐, and Additive‐Free Sulfenylation of Imidazo[1,2‐a]pyridines Using Sulfenamides and an I2 Catalyst

Huijie Qiao, Kun Zhao, Xilin Zhu, Xiaoxu Xu, Chunyang Wang, Lulu Zhong, Shixing Wang, Liting Yang, Dehong Yang, Guoqun Liu, Chunlei Lin and Mingli Jiao

Asian J Org Chem, 2023, 12
DOI: 10.1002/ajoc.202300292

Methylthiolation for Electron‐Rich Heteroarenes with DMSO‐TsCl

Lei‐Yang Zhang, Yue‐Hua Wu, Nai‐Xing Wang, Xue‐Wang Gao, Zhan Yan, Bao‐Cai Xu, Ning Liu, Bo‐Zhou Wang and Yalan Xing

Eur J Org Chem, 2021, 2021, 1446
DOI: 10.1002/ejoc.202100001

Electrochemical regioselective methylthiolation of imidazo[2,1- b ]thiazoles with DMSO

Meng Xiao, Liyu Yi, Wenjie Liu and Gao Cao

Synthetic Communications, 2025, 55, 338
DOI: 10.1080/00397911.2025.2453872

Redox‐Divergent Construction of (Dihydro)thiophenes with DMSO

Heng Liu, Gu‐Cheng He, Chao‐Yang Zhao, Xiang‐Xin Zhang, Ding‐Wei Ji, Yan‐Cheng Hu and Qing‐An Chen

Angew Chem Int Ed, 2021, 60, 24284
DOI: 10.1002/anie.202109026

Metal‐Free Regioselective Chlorosulfenylation of Indoles by Dimethylsulfoxide and 1,2‐Dichloroethane

Kuntal Palit and Niranjan Panda

Eur J Org Chem, 2024, 27
DOI: 10.1002/ejoc.202400110

Direct selenation of imidazoheterocycles and indoles with selenium powder in a copper-catalyzed three-component one-pot system

Tao Guo, Zhe Dong, Panke Zhang, Weiqin Xing and Liping Li

Tetrahedron Letters, 2018, 59, 2554
DOI: 10.1016/j.tetlet.2018.05.046

Recent Developments in Transition‐Metal‐Catalyzed Regioselective Functionalization of Imidazo[1, 2‐a]pyridine

Dipika Konwar and Utpal Bora

ChemistrySelect, 2021, 6, 2716
DOI: 10.1002/slct.202100144

Lewis Acid-Catalyzed Denitrogenative Transannulation of Pyridotriazoles with Nitriles: Synthesis of Imidazopyridines

Abhisek Joshi, Darapaneni Chandra Mohan and Subbarayappa Adimurthy

J. Org. Chem., 2016, 81, 9461
DOI: 10.1021/acs.joc.6b01742

Tandem Flavin-Iodine-Catalyzed Aerobic Oxidative Sulfenylation of Imidazo[1,2-a]Pyridines with Thiols

Hiroki Iida, Ryuta Demizu and Ryoma Ohkado

J. Org. Chem., 2018, 83, 12291
DOI: 10.1021/acs.joc.8b01878

Palladium(II)/Copper(II)‐Catalyzed C–H Sulfidation or Selenation of Arenes Leading to Unsymmetrical Sulfides and Selenides

Kota Nishino, Shouya Tsukahara, Yohei Ogiwara and Norio Sakai

Eur J Org Chem, 2019, 2019, 3815
DOI: 10.1002/ejoc.201900791

Reactivity ofp-Toluenesulfonylmethyl Isocyanide: Iron-Involved C–H Tosylmethylation of Imidazopyridines in Nontoxic Media

Shuai Lu, Xinju Zhu, Ke Li, Yu-Jing Guo, Meng-Dan Wang, Xue-Mei Zhao, Xin-Qi Hao and Mao-Ping Song

J. Org. Chem., 2016, 81, 8370
DOI: 10.1021/acs.joc.6b01552

Iodine-Mediated Sulfenylation of Imidazo[1,2-a]pyridines with Ethyl Arylsulfinates

Jian Sun, Yangxiu Mu, Zafar Iqbal, Jing Hou, Minghua Yang, Zhixiang Yang and Dong Tang

Synlett, 2021, 32, 1014
DOI: 10.1055/a-1396-5933

Hydroxymethylation of active methenyl compounds: DMSO as methylene source and H2O as oxygen source

Liang Zhang, Shuhua Liu, Yunliang Lin and Yuliang Wang

Tetrahedron Letters, 2022, 93, 153663
DOI: 10.1016/j.tetlet.2022.153663

Copper-Catalyzed Three-Component System for Arylsulfenylation of Imidazopyridines with Elemental Sulfur

Chitrakar Ravi, N. Naresh Kumar Reddy, Venkatanarayana Pappula, Supravat Samanta and Subbarayappa Adimurthy

J. Org. Chem., 2016, 81, 9964
DOI: 10.1021/acs.joc.6b01715

Catalyst‐Free Regioselective Sulfenylation of Imidazoheterocycles with Sulfonyl Hydrazides in Water

Soumyadeep Roy Chowdhury, Pulak Fadikar, Injamam Ul Hoque and Soumitra Maity

Asian J Org Chem, 2018, 7, 332
DOI: 10.1002/ajoc.201700670

Investigation of 2-phenylimidazo[1,2- a ]quinolines As Potential Antiproliferative Agents

Shaun W P Rees, Hayden Jones-Moore, Euphemia Leung, David Barker and Lisa I Pilkington

Future Med. Chem., 2023, 15, 229
DOI: 10.4155/fmc-2022-0152

Solvent‐Driven Iodine‐Mediated Oxidative Strategies for the Synthesis of Bis(imidazo[1,2‐a]pyridin‐3‐yl)sulfanes and Disulfanes

S. M. Abdul Shakoor, Devesh S. Agarwal, Sadhika Khullar, Sanjay K. Mandal and Rajeev Sakhuja

Chemistry An Asian Journal, 2017, 12, 3061
DOI: 10.1002/asia.201701274

Organophosphorus‐Catalyzed Deoxygenation of Sulfonyl Chlorides: Electrophilic (Fluoroalkyl)sulfenylation by PIII/PV=O Redox Cycling

Avipsa Ghosh, Morgan Lecomte, Shin‐Ho Kim‐Lee and Alexander T. Radosevich

Angewandte Chemie, 2019, 131, 2890
DOI: 10.1002/ange.201813919

Metal-free direct regioselective thiolation of imidazoheterocycles in water at room temperature

Dulin Kong, Qinghe Wang, Tiao Huang, Min Liang, Qiang Lin and Mingshu Wu

Tetrahedron, 2019, 75, 1457
DOI: 10.1016/j.tet.2019.01.059

Copper(I) Iodide‐Catalyzed Sulfenylation of Maleimides and Related 3‐Indolylmaleimides with Thiols

Zhen‐Hua Yang, Yu‐Long An, Ying Chen, Zhi‐Yu Shao and Sheng‐Yin Zhao

Adv Synth Catal, 2016, 358, 3869
DOI: 10.1002/adsc.201600812

Synthesis of imidazol[1,2-α]pyridine thioethers via using sulfur powder and halides as reactants

Wei Wu, Yingcai Ding, Ping Xie, Qiujie Tang, Charles U. Pittman and Aihua Zhou

Tetrahedron, 2017, 73, 2151
DOI: 10.1016/j.tet.2017.02.065

Electrochemical Oxidative C—H Sulfenylation of Imidazopyridines with Hydrogen Evolution

Yong Yuan, Yangmin Cao, Jin Qiao, Yueping Lin, Xiaomei Jiang, Yaqing Weng, Shan Tang and Aiwen Lei

Chin. J. Chem., 2019, 37, 49
DOI: 10.1002/cjoc.201800405

Dimethyl Sulfoxide: Yesterday's Solvent, Today's Reagent

Zahra Tashrifi, Mohammad Mohammadi Khanaposhtani, Bagher Larijani and Mohammad Mahdavi

Adv Synth Catal, 2020, 362, 65
DOI: 10.1002/adsc.201901021

Sodium Salts (NaI/NaBr/NaCl) for the Halogenation of Imidazo-Fused Heterocycles

Rashmi Semwal, Chitrakar Ravi, Rahul Kumar, Ramavatar Meena and Subbarayappa Adimurthy

J. Org. Chem., 2019, 84, 792
DOI: 10.1021/acs.joc.8b02637

Cross‐Coupling of C−H and N−H Bonds: A Hydrogen Evolution Strategy for the Construction of C−N Bonds

Lekkala Ravindar, Siti Aishah Hasbullah, Nurul Izzaty Hassan and Hua‐Li Qin

Eur J Org Chem, 2022, 2022
DOI: 10.1002/ejoc.202200596

The sulfenylation of imidazopyridines with sulfinic acids mediated by DTBP/HCl

Yu Wang, Hongkun Huang, Xueyu Fang, Chun Ling, Tian Chen, Hua Yao and Zhaohua Yan

Results in Chemistry, 2025, 16, 102428
DOI: 10.1016/j.rechem.2025.102428

Molecular iodine enabled generation of iminyl radicals from oximes: A facile route to imidazo[1,2-a]pyridines and its regioselective C-3 sulfenylated products from simple pyridines

Deepak Singh, Soumyadeep Roy Chowdhury, Shyamal Pramanik and Soumitra Maity

Tetrahedron, 2021, 88, 132125
DOI: 10.1016/j.tet.2021.132125

Transition-Metal-Catalyzed C–S, C–Se, and C–Te Bond Formations via Cross-Coupling and Atom-Economic Addition Reactions. Achievements and Challenges

Irina P. Beletskaya and Valentine P. Ananikov

Chem. Rev., 2022, 122, 16110
DOI: 10.1021/acs.chemrev.1c00836

Photocatalytic sequential C–H functionalization expediting acetoxymalonylation of imidazo heterocycles

Deepak Singh, Shyamal Pramanik and Soumitra Maity

Beilstein J. Org. Chem., 2023, 19, 666
DOI: 10.3762/bjoc.19.48

Recent Advances of C−S Coupling Reaction of (Hetero)Arenes by C−H Functionalization

Lei‐Yang Zhang, Nai‐Xing Wang, Dumitra Lucan, Julia Nastasi and Yalan Xing

The Chemical Record, 2024, 24
DOI: 10.1002/tcr.202400177

ChemInform Abstract: Dual Role of p‐Tosylchloride: Copper‐Catalyzed Sulfenylation and Metal Free Methylthiolation of Imidazo[1,2‐a]pyridines.

Chitrakar Ravi, Darapaneni Chandra Mohan and Subbarayappa Adimurthy

ChemInform, 2016, 47
DOI: 10.1002/chin.201625181

Crystal structure, DFT calculation, Hirshfeld surface analysis and energy framework study of 6-bromo-2-(4-bromophenyl)imidazo[1,2-a]pyridine

Hussien Ahmed Khamees, Kumara Chaluvaiah, Nasseem Ahmed El-khatatneh, Ananda Swamynayaka, Kwong Huey Chong, Jagadeesh Prasad Dasappa and Mahendra Madegowda

Acta Crystallogr E Cryst Commun, 2019, 75, 1620
DOI: 10.1107/S2056989019013410

C3‐Functionalization of Imidazo[1,2‐a]pyridines

Zahra Tashrifi, Mohammad Mohammadi‐Khanaposhtani, Bagher Larijani and Mohammad Mahdavi

Eur J Org Chem, 2020, 2020, 269
DOI: 10.1002/ejoc.201901491

Nickel-catalyzed desulfonative cross-coupling of benzylsulfonyl chlorides with arylsulfonyl chlorides for synthesis of asymmetric thioethers

Ren-Guan Miao, Weiqi Dai, Xinxin Qi and Xiao-Feng Wu

Cell Reports Physical Science, 2023, 4, 101219
DOI: 10.1016/j.xcrp.2022.101219

Redox‐Divergent Construction of (Dihydro)thiophenes with DMSO

Heng Liu, Gu‐Cheng He, Chao‐Yang Zhao, Xiang‐Xin Zhang, Ding‐Wei Ji, Yan‐Cheng Hu and Qing‐An Chen

Angewandte Chemie, 2021, 133, 24486
DOI: 10.1002/ange.202109026

One-Pot, Three-Component Synthesis of 5-Sulfenyl-2-iminothiazolines by Cross-Dehydrogenative C–S Coupling Using I2/DMSO in Open Air

Chandan Bodhak and Animesh Pramanik

J. Org. Chem., 2019, 84, 7265
DOI: 10.1021/acs.joc.9b00785

Iodine‐Catalyzed One‐Pot Decarboxylative Sulfenylation of Electron‐Rich Arenes and Indoles

Chitrakar Ravi, Rashmi Semwal, Rahul Kumar, Narreddula N. K. Reddy and Subbarayappa Adimurthy

ChemistrySelect, 2018, 3, 6116
DOI: 10.1002/slct.201801119

Transition-metal-free methylthiolation of aryl fluorides with S-methylisothiourea sulfate in PEG-400

Xiangmei Wu and Dayun Huang

Tetrahedron, 2025, 184, 134785
DOI: 10.1016/j.tet.2025.134785

One‐Pot Three‐Component Synthesis of Alkylthio‐/Arylthio‐ Substituted Imidazo[1,2‐a]pyridine Derivatives via C(sp2)–H Functionalization

Wenhui Zhu, Yingcai Ding, Zhaogang Bian, Ping Xie, Baojun Xu, Qiujie Tang, Wei Wu and Aihua Zhou

Adv Synth Catal, 2017, 359, 2215
DOI: 10.1002/adsc.201601431

Copper complex supported on the surface of magnetic nanoparticles: an ecofriendly catalyst for C–S and C–Se coupling reactions

Ke Wang and Li-Yuan Chang

J IRAN CHEM SOC, 2024, 21, 1547
DOI: 10.1007/s13738-024-03015-9

Metal-free synthesis of 3-methylthiofurans with homopropargylic alcohols and DMTSM and their friction properties study

Fengqi Fan, Siwei Shen, Kang Zhou, Yuling Wang, Chengcheng Zhang and Rulong Yan

Tetrahedron Letters, 2024, 145, 155157
DOI: 10.1016/j.tetlet.2024.155157

External Oxidant‐Free Oxidative Tandem Cyclization: NaI‐Catalyzed Thiolation for the Synthesis of 3‐Thiosubstituted Pyrroles

Bingxiang Yuan, Yong Jiang, Zhenjie Qi, Xin Guan, Ting Wang and Rulong Yan

Adv Synth Catal, 2019, 361, 5112
DOI: 10.1002/adsc.201900620

S-Aryl Arenesulfonothioate and Copper Acetate Mediated Arylthiolation of 2-Arylpyridines and Heteroarenes

Poonam Sharma and Nidhi Jain

J. Org. Chem., 2019, 84, 13045
DOI: 10.1021/acs.joc.9b01954