Novel intramolecular π–π-interaction in a BODIPY system by oxidation of a single selenium center: geometrical stamping and spectroscopic and spectrometric distinctions

Youngsam Kim, Taehong Jun, Sandip V. Mulay, Sudesh T. Manjare, Jinseong Kwak, Yunho Lee and David G. Churchill

Dalton Trans., 2017, 46, 4111
DOI: 10.1039/C7DT00555E

Thiol modifier effects of diphenyl diselenides: insight from experiment and DFT calculations

Pablo A. Nogara, Cláudia S. Oliveira, Andrea Madabeni, Marco Bortoli, João Batista T. Rocha and Laura Orian

New J. Chem., 2023, 47, 5796
DOI: 10.1039/D2NJ05976B

From a humorous post to a detailed quantum-chemical study: isocyanate synthesis revisited

Oleg B. Beletsan, Igor Gordiy, Sergey S. Lunkov, Mikhail A. Kalinin, Larisa E. Alkhimova, Egor A. Nosach, Egor A. Ilin, Alexandr V. Bespalov, Olgert L. Dallakyan, Aleksandr A. Chamkin, Ilya V. Prolomov, Radion A. Zaripov, Andrey A. Pershin, Bogdan O. Protsenko, Yury V. Rusalev, Ruslan A. Oganov, Diana K. Kovaleva, Vladimir A. Mironov, Victor V. Dotsenko, Alexandr M. Genaev, Dmitry I. Sharapa and Denis S. Tikhonov

Phys. Chem. Chem. Phys., 2024, 26, 13850
DOI: 10.1039/D3CP04654K

Three-component aminoselenation of alkenes via visible-light enabled Fe-catalysis

Binbin Huang, Yanan Li, Chao Yang and Wujiong Xia

Green Chem., 2020, 22, 2804
DOI: 10.1039/C9GC04163J

Visible-light induced selenocyclization of 2-ethynylanilines under ambient conditions: simple FeBr3 as a dual-functional catalyst

Binbin Huang, Xinye Tang, Jiawei Yuan, Mingyu Zhang, Zhenyu Luo, Junlei Wang and Caicai Lu

Org. Biomol. Chem., 2024, 22, 6198
DOI: 10.1039/D4OB01062K

Continuous flow synthesis of 2,2′-diselenobis(benzoic acid) and derivatives

Francesca Begini, Dorota Krasowska, Aleksandra Jasiak, Jozef Drabowicz, Claudio Santi and Luca Sancineto

React. Chem. Eng., 2020, 5, 641
DOI: 10.1039/D0RE00012D

Sequential oxidations of phenylchalcogenides by H2O2: insights into the redox behavior of selenium via DFT analysis

Marco Bortoli, Matteo Bruschi, Marcel Swart and Laura Orian

New J. Chem., 2020, 44, 6724
DOI: 10.1039/C9NJ06449D

Recyclable (PhSe)2-catalyzed selective oxidation of isatin by H2O2: a practical and waste-free access to isatoic anhydride under mild and neutral conditions

Lei Yu, Jianqing Ye, Xu Zhang, Yuanhua Ding and Qing Xu

Catal. Sci. Technol., 2015, 5, 4830
DOI: 10.1039/C5CY01030F

One-pot cascade polymerization based on the addition reactions of electrophilic selenium reagents to alkenes

Xiaowei An, Weihong Lu, Minglun Pang, Zhengbiao Zhang, Xiulin Zhu, Jian Zhu and Xiangqiang Pan

Polym. Chem., 2019, 10, 574
DOI: 10.1039/C8PY01441H

Synthesis, characterization and antioxidant activity of organoselenium and organotellurium compound derivatives of chrysin

Sergio F. Fonseca, David B. Lima, Diego Alves, Raquel G. Jacob, Gelson Perin, Eder João Lenardão and Lucielli Savegnago

New J. Chem., 2015, 39, 3043
DOI: 10.1039/C4NJ02329C

On the coordination behaviour of diorganoselenium ligands based on amino and azole functionalities: silver(i) complexes with relevance for biological applications

Roxana A. Popa, Maria David, Emilia Licarete, Manuela Banciu and Anca Silvestru

New J. Chem., 2022, 46, 23019
DOI: 10.1039/D2NJ04812D

Efficient oxyselenation and aminoselenation utilizing a selenenyl iodide based on the characteristic thermodynamics of its reaction with olefins

Satoru Kuwano, Erika Takahashi, Jun Kikushima, Shohei Sase and Kei Goto

New J. Chem., 2023, 47, 9569
DOI: 10.1039/D2NJ06346H

Fused multifunctionalized dibenzoselenophenes from tetraynes

Yimin Hu, Jie Ma, Lidong Li, Qiong Hu, Shuang Lv, Baohua Liu and Shaowu Wang

Chem. Commun., 2017, 53, 1542
DOI: 10.1039/C6CC09732D

New selenosteroids as antiproliferative agents

Alma Fuentes-Aguilar, Laura L. Romero-Hernández, Ailed Arenas-González, Penélope Merino-Montiel, Sara Montiel-Smith, Socorro Meza-Reyes, José Luis Vega-Báez, Gabriela B. Plata, José M. Padrón, Óscar López and José G. Fernández-Bolaños

Org. Biomol. Chem., 2017, 15, 5041
DOI: 10.1039/C7OB00458C

A facile approach to constructing Pd@PCN–Se nano-composite catalysts for selective alcohol oxidation reactions

Kuanhong Cao, Xin Deng, Tian Chen, Qitao Zhang and Lei Yu

J. Mater. Chem. A, 2019, 7, 10918
DOI: 10.1039/C9TA00846B

Organoselenium-catalyzed selectivity-switchable oxidation of β-ionone

Lei Yu, Zengbing Bai, Xu Zhang, Xiaohong Zhang, Yuanhua Ding and Qing Xu

Catal. Sci. Technol., 2016, 6, 1804
DOI: 10.1039/C5CY01395J

Design and preparation of a polymer resin-supported organoselenium catalyst with industrial potential

Yuguang Wang, Lihua Yu, Bingchun Zhu and Lei Yu

J. Mater. Chem. A, 2016, 4, 10828
DOI: 10.1039/C6TA02566H

Synergetic catalysis of Se and Cu allowing diethoxylation of halomethylene ketones using O2 as the mild oxidant

Zhicheng Cao, Xin Deng, Chao Chen, Yonghong Liu, Lei Yu and Xuefeng Jiang

React. Chem. Eng., 2021, 6, 454
DOI: 10.1039/D0RE00471E

Metal- and photocatalyst-free synthesis of 3-selenylindoles and asymmetric diarylselenides promoted by visible light

Ignacio D. Lemir, Willber D. Castro-Godoy, Adrián A. Heredia, Luciana C. Schmidt and Juan E. Argüello

RSC Adv., 2019, 9, 22685
DOI: 10.1039/C9RA03642C

Selenium-containing BODIPY dyes as photosensitizers for triplet–triplet annihilation upconversion

Mika Nakashima, Keita Iizuka, Masanobu Karasawa, Kazuyuki Ishii and Yuji Kubo

J. Mater. Chem. C, 2018, 6, 6208
DOI: 10.1039/C8TC00944A

Silver-catalyzed direct selanylation of indoles: synthesis and mechanistic insights

Elise Ane Maluf Rios, Carla M. B. Gomes, Gabriel L. Silvério, Eduardo Q. Luz, Sher Ali, Caroline da Ros Montes D'Oca, Breidi Albach, Renan B. Campos and Daniel S. Rampon

RSC Adv., 2023, 13, 914
DOI: 10.1039/D2RA06813C

Electrochemical selenocyclization of 2-ethynylanilines with diselenides: facile and efficient access to 3-selenylindoles

Mingyu Zhang, Zhenyu Luo, Xinye Tang, Linmin Yu, Jinglin Pei, Junlei Wang, Caicai Lu and Binbin Huang

Org. Biomol. Chem., 2023, 21, 8918
DOI: 10.1039/D3OB01502E

Phenylselanyl-1H-1,2,3-triazole-4-carbonitriles: synthesis, antioxidant properties and use as precursors to highly functionalized tetrazoles

Lucielli Savegnago, Manoela do Sacramento, Lucimar M. P. Brod, Mariana G. Fronza, Natália Seus, Eder J. Lenardão, Márcio W. Paixão and Diego Alves

RSC Adv., 2016, 6, 8021
DOI: 10.1039/C5RA22445D

Synthesis of benzo[b]chalcogenophenes fused to selenophenes via intramolecular electrophilic cyclization of 1,3-diynes

Paola S. Hellwig, Jonatan S. Guedes, Angelita M. Barcellos, Raquel G. Jacob, Claudio C. Silveira, Eder J. Lenardão and Gelson Perin

Org. Biomol. Chem., 2021, 19, 596
DOI: 10.1039/D0OB02362K

Selenium-catalyzed selective reactions of carbonyl derivatives: state-of-the-art and future challenges

Xinrui Xiao, Cheng Guan, Jie Xu, Weijun Fu and Lei Yu

Green Chem., 2021, 23, 4647
DOI: 10.1039/D1GC00961C

Naturally occurring prenylated flavonoids from African Erythrina plant species

Bienvenu Tsakem, Fidele Ntie Kang, Rémy Bertrand Teponno and Xavier Siwe Noundou

RSC Adv., 2025, 15, 27816
DOI: 10.1039/D5RA03457D

Synthesis of enantiomerically pure bis(2,2-dimethyl-1,3-dioxolanylmethyl)chalcogenides and dichalcogenides

Elton L. Borges, Thiago J. Peglow, Márcio S. Silva, Caroline G. Jacoby, Paulo H. Schneider, Eder J. Lenardão, Raquel G. Jacob and Gelson Perin

New J. Chem., 2016, 40, 2321
DOI: 10.1039/C5NJ02945G

Selenium-catalyzed oxidation of alkenes: insight into the mechanisms and developing trend

Hongen Cao, Rongrong Qian and Lei Yu

Catal. Sci. Technol., 2020, 10, 3113
DOI: 10.1039/D0CY00400F

Organoselenium small molecules as catalysts for the oxidative functionalization of organic molecules

Vandana Rathore, Cavya Jose and Sangit Kumar

New J. Chem., 2019, 43, 8852
DOI: 10.1039/C9NJ00964G

Synthesis and triplet sensitization of bis(arylselanyl)BOPHYs; potential application in triplet–triplet annihilation upconversion

Ryohei Hasegawa, Shinji Iwakiri and Yuji Kubo

New J. Chem., 2021, 45, 6091
DOI: 10.1039/D1NJ00721A

Metal and non-metal oxide-supported selenium as potential industrial catalysts

Meng Ge, Tao Ju, Yiyang Zhang and Daming Yong

React. Chem. Eng., 2025, 10, 1730
DOI: 10.1039/D5RE00066A

PhSe(O)OH/Al(NO3)3-Catalyzed selectivity controllable oxidation of sulphide owing to the synergistic effect of Se, Al3+and nitrate

Xu Zhang, Rui Zhou, Zhengyuan Qi, Liping Chen and Lei Yu

React. Chem. Eng., 2022, 7, 1990
DOI: 10.1039/D2RE00190J

Recent progress in selenium-catalyzed organic reactions

Lixiong Shao, Yiming Li, Jianmei Lu and Xuefeng Jiang

Org. Chem. Front., 2019, 6, 2999
DOI: 10.1039/C9QO00620F

Catalytic epoxidation of β-ionone with molecular oxygen using selenium-doped silica materials

Peizi Li, Kuanhong Cao, Xiaobi Jing, Yonghong Liu and Lei Yu

New J. Chem., 2021, 45, 17241
DOI: 10.1039/D1NJ03311E

Fabrication of Se/C using carbohydrates as biomass starting materials: an efficient catalyst for regiospecific epoxidation of β-ionone with ultrahigh turnover numbers

Yufan Yang, Xin Fan, Hongen Cao, Sainan Chu, Xu Zhang, Qing Xu and Lei Yu

Catal. Sci. Technol., 2018, 8, 5017
DOI: 10.1039/C8CY01413B

Organoselenium-catalyzed synthesis of indoles through intramolecular C–H amination

Xuelin Zhang, Ruizhi Guo and Xiaodan Zhao

Org. Chem. Front., 2015, 2, 1334
DOI: 10.1039/C5QO00179J

A cost‐effective shortcut to prepare organoselenium catalysts via decarboxylative coupling of phenylacetic acid with elemental selenium

Hongen Cao, Mingxuan Liu, Rongrong Qian, Xu Zhang and Lei Yu

Applied Organom Chemis, 2019, 33
DOI: 10.1002/aoc.4599

Meet Our Editor-in-Chief

Claudio Santi

CCB, 2020, 14, 69
DOI: 10.2174/221279681402201119090048

Synthesis and anticancer activity of bis(2-arylimidazo[1,2-a]pyridin-3-yl) selenides and diselenides: the copper-catalyzed tandem C–H selenation of 2-arylimidazo[1,2-a]pyridine with selenium

Mio Matsumura, Tsutomu Takahashi, Hikari Yamauchi, Shunsuke Sakuma, Yukako Hayashi, Tadashi Hyodo, Tohru Obata, Kentaro Yamaguchi, Yasuyuki Fujiwara and Shuji Yasuike

Beilstein J. Org. Chem., 2020, 16, 1075
DOI: 10.3762/bjoc.16.94

“Green Is the Color”: An Update on Ecofriendly Aspects of Organoselenium Chemistry

Juliano B. Azeredo, Filipe Penteado, Vanessa Nascimento, Luca Sancineto, Antonio L. Braga, Eder João Lenardao and Claudio Santi

Molecules, 2022, 27, 1597
DOI: 10.3390/molecules27051597

Organoselenium-Catalyzed Synthesis of Oxygen- and Nitrogen-Containing Heterocycles

Ruizhi Guo, Jiachen Huang, Haiyan Huang and Xiaodan Zhao

Org. Lett., 2016, 18, 504
DOI: 10.1021/acs.orglett.5b03543

Mesoporous Mn‐Se/Al2O3: A recyclable and reusable catalyst for selective oxidation of alcohols

Yan Zeng, Tian Chen, Xu Zhang, Ying Chen, Hongwei Zhou and Lei Yu

Applied Organom Chemis, 2022, 36
DOI: 10.1002/aoc.6658

Synthesis of Thiol Esters Using PhSZnBr as Sulfenylating Agent: A DFT‐Guided Optimization of Reaction Conditions

Luca Sancineto, Caterina Tidei, Luana Bagnoli, Francesca Marini, Vito Lippolis, Massimiliano Arca, Eder João Lenardão and Claudio Santi

Eur J Org Chem, 2016, 2016, 2999
DOI: 10.1002/ejoc.201600366

Selenium-directed synthesis of Pd nanoparticles on mesoporous silica-coated Fe3O4: An efficient magnetic catalyst for oxidative alkene cracking

Zhida Zhu, Wenjun Wang, Li Zeng, Fan Zhang and Jingjing Liu

Catalysis Communications, 2020, 142, 106031
DOI: 10.1016/j.catcom.2020.106031

Design and Preparation of Poly‐Selenides: Easily Fabricated and Efficient Organoselenium Materials for Heavy Metal Removing and Recycling

Xiaobi Jing, Changzhou Chen, Xin Deng, Xu Zhang, Duo Wei and Lei Yu

Applied Organom Chemis, 2018, 32
DOI: 10.1002/aoc.4332

FeCl3-catalyzed three-component aryl-selenylation of alkenes

Chao Xu, Ze He, Hongqin Yang, Hongyi Chen and Qingle Zeng

Tetrahedron, 2021, 91, 132239
DOI: 10.1016/j.tet.2021.132239

Mono and Dinuclear Palladium Pincer Complexes of NNSe Ligand as a Catalyst for Decarboxylative Direct C−H Heteroarylation of (Hetero)arenes

Sohan Singh, Vikki N. Shinde, Sunil Kumar, Neha Meena, Nattamai Bhuvanesh, Krishnan Rangan, Anil Kumar and Hemant Joshi

Chemistry An Asian Journal, 2023, 18
DOI: 10.1002/asia.202300628

Computational modeling of the catalytic cycle of the di-chalcogenide compounds in the capture and release of carbon dioxide: effect of temperature and substitution on the catalytic activity

Ramesh Kheirabadi, Mohammad Vakili, Razieh Morad and Malik Maaza

J IRAN CHEM SOC, 2022, 19, 3963
DOI: 10.1007/s13738-022-02578-9

Trichloroisocyanuric Acid (TCCA): A Suitable Reagent for the Synthesis of Selanyl‐benzo[b]chalcogenophenes

Gustavo B. Blödorn, Luis Fernando B. Duarte, Juliano A. Roehrs, Márcio S. Silva, José S. S. Neto and Diego Alves

Eur J Org Chem, 2022, 2022
DOI: 10.1002/ejoc.202200775

Ferrocenyl chalcogeno (sugar) triazole conjugates: Synthesis, characterization and anticancer properties

Sangeetha Panaka, Rajiv Trivedi, K. Jaipal, L. Giribabu, P. Sujitha, C. Ganesh Kumar and B. Sridhar

Journal of Organometallic Chemistry, 2016, 813, 125
DOI: 10.1016/j.jorganchem.2016.04.011

Dehydration of Aldoximes Using PhSe(O)OH as the Pre-Catalyst in Air

Xu Zhang, Jingjing Sun, Yuanhua Ding and Lei Yu

Org. Lett., 2015, 17, 5840
DOI: 10.1021/acs.orglett.5b03011

ROS-Scavenging Selenofluoxetine Derivatives Inhibit In Vivo Serotonin Reuptake

Giovanni Ribaudo, Marco Bortoli, Colby E. Witt, Brenna Parke, Sergio Mena, Erika Oselladore, Giuseppe Zagotto, Parastoo Hashemi and Laura Orian

ACS Omega, 2022, 7, 8314
DOI: 10.1021/acsomega.1c05567

Selenium-incorporated polymeric carbon nitride for visible-light photocatalytic regio-specific epoxidation of β-ionone

Hongjia Li, Hongen Cao, Tian Chen, Xu Zhang and Yaocheng Shi

Molecular Catalysis, 2020, 483, 110715
DOI: 10.1016/j.mcat.2019.110715

DES as a green solvent to prepare 1,2-bis-organylseleno alkenes. Scope and limitations

Eric F. Lopes, Lóren C. Gonçalves, Julio C.G. Vinueza, Raquel G. Jacob, Gelson Perin, Claudio Santi and Eder J. Lenardão

Tetrahedron Letters, 2015, 56, 6890
DOI: 10.1016/j.tetlet.2015.10.095

Synthesis of 5H‐Selenopheno[3,2‐c]isochromen‐5‐ones Promoted by Dialkyl Diselenides and Oxone®

Helen A. Goulart, José S. S. Neto, Angelita M. Barcellos, Thiago Barcellos, Márcio S. Silva, Diego Alves, Raquel G. Jacob, Eder J. Lenardão and Gelson Perin

Adv Synth Catal, 2019, 361, 3403
DOI: 10.1002/adsc.201900288

Organoboron compounds as versatile reagents in the transition metal-catalyzed C–S, C–Se and C–Te bond formation

Angelita M. Barcellos, Manoela Sacramento, Gabriel P. da Costa, Gelson Perin, Eder João Lenardão and Diego Alves

Coordination Chemistry Reviews, 2021, 442, 214012
DOI: 10.1016/j.ccr.2021.214012

One-pot synthesis of 1,2,4-oxadiazoles from chalcogen amino acid derivatives under microwave irradiation

Lucas Wolf, João C.P. Mayer, Natália Quoos, André C. Sauer, Ricardo S. Schwab, Oscar E.D. Rodrigues and Luciano Dornelles

Tetrahedron, 2021, 91, 132222
DOI: 10.1016/j.tet.2021.132222

Synthesis of Organochalcogen Compounds using Non-Conventional Reaction Media

Gelson Perin, Diego Alves, Raquel G. Jacob, Angelita M. Barcellos, Liane K. Soares and Eder J. Lenardão

ChemistrySelect, 2016, 1, 205
DOI: 10.1002/slct.201500031

[Tc(NO)Cl2(PPh3)2(CH3CN)] and Its Reactions with 2,2′-Dipyridyl Dichalcogenides

Till Erik Sawallisch, Susanne Margot Rupf, Abdullah Abdulkader, Moritz Johannes Ernst, Maximilian Roca Jungfer and Ulrich Abram

Molecules, 2025, 30, 793
DOI: 10.3390/molecules30040793

Mechanistic Studies on the Anodic Functionalization of Alkenes Catalyzed by Diselenides

Mona Wilken, Stefan Ortgies, Alexander Breder and Inke Siewert

ACS Catal., 2018, 8, 10901
DOI: 10.1021/acscatal.8b01236

In the Chalcogenoxide Elimination Panorama: Systematic Insight into a Key Reaction

Andrea Madabeni, Simone Zucchelli, Pablo A. Nogara, João B. T. Rocha and Laura Orian

J. Org. Chem., 2022, 87, 11766
DOI: 10.1021/acs.joc.2c01454

Electrophilic Selenium Catalysis with Electrophilic N-F Reagents as the Oxidants

Ruizhi Guo, Lihao Liao and Xiaodan Zhao

Molecules, 2017, 22, 835
DOI: 10.3390/molecules22050835

Sonochemistry: An efficient alternative to the synthesis of 3-selanylindoles using CuI as catalyst

Beatriz M. Vieira, Samuel Thurow, Juliana S. Brito, Gelson Perin, Diego Alves, Raquel G. Jacob, Claudio Santi and Eder J. Lenardão

Ultrasonics Sonochemistry, 2015, 27, 192
DOI: 10.1016/j.ultsonch.2015.05.012

Copper‐catalyzed C−H Selenation of 2‐Substituted Benzo[b]furans with Diaryl Diselenides: Synthesis of 2‐Substituted 3‐Selanylbenzo[b]furan Derivatives

Yuki Murata, Naoaki Otake, Moeko Sano, Mio Matsumura and Shuji Yasuike

Asian J Org Chem, 2021, 10, 2975
DOI: 10.1002/ajoc.202100527

Design, Synthesis, and Biological Evaluation of Novel Hydroxamic Acid-Based Organoselenium Hybrids

Jameelah S. Alotaibi, Yasair S. Al-Faiyz and Saad Shaaban

Pharmaceuticals, 2023, 16, 367
DOI: 10.3390/ph16030367

Organotellurium catalysis-enabled utilization of molecular oxygen as oxidant for oxidative deoximation reactions under solvent-free conditions

Xin Deng, Hongen Cao, Chao Chen, Hongwei Zhou and Lei Yu

Science Bulletin, 2019, 64, 1280
DOI: 10.1016/j.scib.2019.07.007

Direct Synthesis of 4‐Organylselanylpyrazoles by Copper‐ Catalyzed One‐Pot Cyclocondensation and CH Bond Selenylation Reactions

Daniela H. Oliveira, Thalita B. Aquino, José Edmilson R. Nascimento, Gelson Perin, Raquel G. Jacob and Diego Alves

Adv Synth Catal, 2015, 357, 4041
DOI: 10.1002/adsc.201500625

Selenium-doped Fe2O3-catalyzed oxidative scission of C C bond

Chuang Liu, Jinfei Mao, Xu Zhang and Lei Yu

Catalysis Communications, 2020, 133, 105828
DOI: 10.1016/j.catcom.2019.105828

Solid-State 77Se NMR of Organoselenium Compounds through Cross Polarization Magic Angle Spinning (CPMAS) Method

Duo Wei, Mengting Han and Lei Yu

Sci Rep, 2017, 7
DOI: 10.1038/s41598-017-06892-8

Copper-catalyzed three-component reaction of ethynylstibanes, organic azides, and selenium: A simple and efficient synthesis of novel selenides and diselenides having 1,2,3-triazole rings

Mizuki Yamada, Mio Matsumura, Erina Sakaki, Shih-yun Yen, Masatoshi Kawahata, Tadashi Hyodo, Kentaro Yamaguchi, Yuki Murata and Shuji Yasuike

Tetrahedron, 2019, 75, 1406
DOI: 10.1016/j.tet.2019.01.056

Ebselen-Agents for Sensing, Imaging and Labeling: Facile and Full-Featured Application in Biochemical Analysis

Jiawei Zhang, Lei Yang, Yuxin Wang, Tianyi Cao, Zhiwei Sun, Jie Xu, Yuxia Liu and Guang Chen

ACS Appl. Bio Mater., 2021, 4, 2217
DOI: 10.1021/acsabm.0c01561

Selenization of cotton products with NaHSe endowing the antibacterial activities

Mingxuan Liu, Xiaoling Zhang, Sainan Chu, Yanyu Ge, Tao Huang, Yonghong Liu and Lei Yu

Chinese Chemical Letters, 2022, 33, 205
DOI: 10.1016/j.cclet.2021.05.061

A scalable production of anisonitrile through organoselenium-catalyzed dehydration of anisaldoxime under solventless conditions

Xiaobi Jing, Tingting Wang, Yuanhua Ding and Lei Yu

Applied Catalysis A: General, 2017, 541, 107
DOI: 10.1016/j.apcata.2017.05.007

Photocatalytic Aerobic Phosphatation of Alkenes

Christian Depken, Felix Krätzschmar, Rene Rieger, Katharina Rode and Alexander Breder

Angew Chem Int Ed, 2018, 57, 2459
DOI: 10.1002/anie.201711599

PhSe(O)OH/NHPI-catalyzed oxidative deoximation reaction using air as oxidant

Feng Wang, Chenggen Yang, Yaocheng Shi and Lei Yu

Molecular Catalysis, 2021, 514, 111849
DOI: 10.1016/j.mcat.2021.111849

Organoselenium‐Catalyzed Oxidative Ring Expansion of Methylenecyclopropanes with Hydrogen Peroxide

Lei Yu, Fenglin Chen and Yuanhua Ding

ChemCatChem, 2016, 8, 1033
DOI: 10.1002/cctc.201501309

Copper-catalyzed tandem cyclization of 2-(2-iodophenyl)imidazo[1,2-a]pyridine derivatives with selenium: Synthesis of benzo[b]selenophene-fused imidazo[1,2-a]pyridines

Mio Matsumura, Yumi Sakata, Atsuya Iwase, Masatoshi Kawahata, Yuki Kitamura, Yuki Murata, Naoki Kakusawa, Kentaro Yamaguchi and Shuji Yasuike

Tetrahedron Letters, 2016, 57, 5484
DOI: 10.1016/j.tetlet.2016.10.095

Metal Catalysis in Thiolation and Selenation Reactions of Alkynes Leading to Chalcogen-Substituted Alkenes and Dienes

Nikolai V. Orlov

ChemistryOpen, 2015, 4, 682
DOI: 10.1002/open.201500137

Organoselenium-Catalyzed Conversion of Oximes to Nitriles or Ketones

Liming Wang, Ke Li and Wanxuan Zhang

Chinese Journal of Organic Chemistry, 2022, 42, 1235
DOI: 10.6023/cjoc202109036

Organoselenium Compounds as Phytochemicals from the Natural Kingdom

Hanane Achibat, Nohad A AlOmari, Federica Messina, Luca Sancineto, Mostafa Khouili and Claudio Santi

Natural Product Communications, 2015, 10
DOI: 10.1177/1934578X1501001119

50 Years of Organoselenium Chemistry, Biochemistry and Reactivity: Mechanistic Understanding, Successful and Controversial Stories

Andrea Madabeni, Marco Bortoli, Pablo A. Nogara, Giovanni Ribaudo, Marco Dalla Tiezza, Leopold Flohé, João B. T. Rocha and Laura Orian

Chemistry A European J, 2024, 30
DOI: 10.1002/chem.202403003

Selenium Catalyzed Oxidation of Aldehydes: Green Synthesis of Carboxylic Acids and Esters

Luca Sancineto, Caterina Tidei, Luana Bagnoli, Francesca Marini, Eder Lenardão and Claudio Santi

Molecules, 2015, 20, 10496
DOI: 10.3390/molecules200610496

Homoleptic and heteroleptic diorganoselenides containing pyrazole functionalities. Synthesis, characterization, and antioxidant activity

Roxana A. Popa, Adrian Nicoară, Massimiliano Arca, Vito Lippolis, Anna Pintus and Anca Silvestru

Applied Organom Chemis, 2022, 36
DOI: 10.1002/aoc.6894

Reaction mechanism of organoselenium-catalyzed syn-dichlorination of alkenes: a DFT study

Lijun Fu, Xueli Mu and Baiqing Li

J Mol Model, 2018, 24
DOI: 10.1007/s00894-018-3624-9

Synthesis of enantiomerically pure glycerol derivatives containing an organochalcogen unit: In vitro and in vivo antioxidant activity

Patrick C. Nobre, Henrique A. Vargas, Caroline G. Jacoby, Paulo H. Schneider, Angela M. Casaril, Lucielli Savegnago, Ricardo F. Schumacher, Eder J. Lenardão, Daiana S. Ávila, Luiz B.L. Rodrigues Junior and Gelson Perin

Arabian Journal of Chemistry, 2020, 13, 883
DOI: 10.1016/j.arabjc.2017.08.007

Silver-catalyzed direct selenylation of terminal alkynes through C H bond functionalization

Maurício C.D.F. Xavier, Bruna Goldani, Ricardo F. Schumacher, Gelson Perin, Paulo Henrique Schneider and Diego Alves

Molecular Catalysis, 2017, 427, 73
DOI: 10.1016/j.molcata.2016.11.033

Organoselenium-Catalyzed Oxidative C═C Bond Cleavage: A Relatively Green Oxidation of Alkenes into Carbonyl Compounds with Hydrogen Peroxide

Tingting Wang, Xiaobi Jing, Chao Chen and Lei Yu

J. Org. Chem., 2017, 82, 9342
DOI: 10.1021/acs.joc.7b01245

Recent Advances in the Synthesis of Selenophenes and Their Derivatives

Paola S. Hellwig, Thiago J. Peglow, Filipe Penteado, Luana Bagnoli, Gelson Perin and Eder J. Lenardão

Molecules, 2020, 25, 5907
DOI: 10.3390/molecules25245907

Photokatalytische aerobe Phosphatierung von Alkenen

Christian Depken, Felix Krätzschmar, Rene Rieger, Katharina Rode and Alexander Breder

Angewandte Chemie, 2018, 130, 2484
DOI: 10.1002/ange.201711599

Iron‐Enabled Utilization of Air as the Terminal Oxidant Leading to Aerobic Oxidative Deoximation by Organoselenium Catalysis

Chao Chen, Xu Zhang, Hongen Cao, Fang Wang, Lei Yu and Qing Xu

Adv Synth Catal, 2019, 361, 603
DOI: 10.1002/adsc.201801163

Carbon-based selenium: an easily fabricated environmental material for removing lead from the electrolytic wastewater

Zhida Zhu, Shuai Sun and Xiaobi Jing

Chem. Pap., 2022, 76, 401
DOI: 10.1007/s11696-021-01875-6

Fluorescent Benzoselenadiazoles: Synthesis, Characterization, and Quantification of Intracellular Lipid Droplets and Multicellular Model Staining

Ingryd R. Medeiros, José R. Corrêa, Ana L. A. Barbosa, Roberta Krüger, Renata A. Balaguez, Thiago O. Lopes, Heibbe C. B. de Oliveira, Diego Alves and Brenno A. D. Neto

J. Org. Chem., 2020, 85, 10561
DOI: 10.1021/acs.joc.0c01031

One-pot modular synthesis of β-chalcogen amides via regioselective 2-oxazolines ring-opening reaction promoted by indium chalcogenolates under microwave irradiation

Larissa F. Guimarães, Luana Bettanin, Roberth N. da Trindade, Cleiton da Silva, Andrielli Leitemberger, Marcelo Godoi and Fábio Z. Galetto

Tetrahedron Letters, 2020, 61, 152180
DOI: 10.1016/j.tetlet.2020.152180

Celebrating Two Centuries of Research in Selenium Chemistry: State of the Art and New Prospective

Claudio Santi and Luana Bagnoli

Molecules, 2017, 22, 2124
DOI: 10.3390/molecules22122124

Asymmetric Catalysis of Chiral Bifunctional Selenides and Selenonium Salts Bearing a Urea Group

Ken Okuno, Takumi Nakamura and Seiji Shirakawa

Asian J Org Chem, 2021, 10, 655
DOI: 10.1002/ajoc.202100001

New Dimensions in Rongalite Chemistry: The Land of Opportunities in Organic Synthesis and Material Sciences

Rashid Ali

ChemistrySelect, 2020, 5, 10795
DOI: 10.1002/slct.202002878

Ultrasound‐Assisted Multicomponent Reactions, Organometallic and Organochalcogen Chemistry

Filipe Penteado, Bonifacio Monti, Luca Sancineto, Gelson Perin, Raquel G. Jacob, Claudio Santi and Eder J. Lenardão

Asian J Org Chem, 2018, 7, 2368
DOI: 10.1002/ajoc.201800477

Isolation and derivatization of bioactive compounds from Saussurea lappa roots with antifungal efficacy against plant pathogenic fungi

Rupinder Kaur, Ramandeep Kaur, Ravinder Singh, Urvashi Bhardwaj and Parul Sharma

Journal of Biologically Active Products from Nature, 2024, 14, 551
DOI: 10.1080/22311866.2024.2434569

Organoselenium‐Catalyzed Baeyer–Villiger Oxidation of α,β‐Unsaturated Ketones by Hydrogen Peroxide to Access Vinyl Esters

Xu Zhang, Jianqing Ye, Lei Yu, Xinkang Shi, Ming Zhang, Qing Xu and Mark Lautens

Adv Synth Catal, 2015, 357, 955
DOI: 10.1002/adsc.201400957

Efficient Selenium‐Catalyzed Selective C(sp3)−H Oxidation of Benzylpyridines with Molecular Oxygen

Weiwei Jin, Poonnapa Zheng, Wing‐Tak Wong and Ga‐Lai Law

Adv Synth Catal, 2017, 359, 1588
DOI: 10.1002/adsc.201601065

Rise of diselenides: Recent advances in the synthesis of heteroarylselenides

Anna Ivanova and Pavel Arsenyan

Coordination Chemistry Reviews, 2018, 370, 55
DOI: 10.1016/j.ccr.2018.05.015

Synthesis and Evaluation of Antioxidant, Anti‐Edematogenic and Antinociceptive Properties of Selenium‐Sulfa Compounds

Manoela Sacramento, Angélica S. Reis, Carolina C. Martins, Cristiane Luchese, Ethel A. Wilhelm and Diego Alves

ChemMedChem, 2022, 17
DOI: 10.1002/cmdc.202100507

Synthesis of l-Selenocysteine and α-Methyl-l-Selenocysteine Derivatives Using Woollins’ Reagent and Their Application as Chiral Selenium Catalysts

Michio Iwaoka, Shun Ito, Izumo Miyazaki and Momoko Michibata

Proc. Natl. Acad. Sci., India, Sect. A Phys. Sci., 2016, 86, 499
DOI: 10.1007/s40010-016-0307-8

Cobaltoceniumselenolate Gold(I) Complexes: Synthesis, Spectroscopic, Structural and Anticancer Properties

Daniel Menia, Holger Kopacka, Klaus Wurst, Thomas Müller, Petra Lippmann, Ingo Ott and Benno Bildstein

Eur J Inorg Chem, 2021, 2021, 2784
DOI: 10.1002/ejic.202100379

Recent Developments in the Synthesis of Organoselenium Compounds Based on the Reactions of Organic Diselenides with Acetylenes

Maxim V. Musalov, Vladimir A. Potapov, Maria V. Musalova, Svetlana V. Amosova and Leonid B. Krivdin

Catalysts, 2023, 13, 1369
DOI: 10.3390/catal13101369

Glycerol as Precursor of Organoselanyl and Organotellanyl Alkynes

Eder Lenardão, Elton Borges, Guilherme Stach, Liane Soares, Diego Alves, Ricardo Schumacher, Luana Bagnoli, Francesca Marini and Gelson Perin

Molecules, 2017, 22, 391
DOI: 10.3390/molecules22030391

Zinc-Selenium reagents in organic synthesis

Claudio Santi, Lucia Capoccia and Bonifacio Monti

Physical Sciences Reviews, 2018, 3
DOI: 10.1515/psr-2017-0129

Addition–Elimination or Nucleophilic Substitution? Understanding the Energy Profiles for the Reaction of Chalcogenolates with Dichalcogenides

Marco Bortoli, Lando P. Wolters, Laura Orian and F. Matthias Bickelhaupt

J. Chem. Theory Comput., 2016, 12, 2752
DOI: 10.1021/acs.jctc.6b00253

ChemInform Abstract: “The Green Side of the Moon: Ecofriendly Aspects of Organoselenium Chemistry”

Stefano Santoro, Juliano B. Azeredo, Vanessa Nascimento, Luca Sancineto, Antonio L. Braga and Claudio Santi

ChemInform, 2014, 45
DOI: 10.1002/chin.201447263

AIBN‐Initiated Oxidative Deoximation Reaction: A Metal‐Free and Environmentally‐Friendly Protocol

Feng Wang, Tian Chen, Yaocheng Shi and Lei Yu

Asian J Org Chem, 2021, 10, 614
DOI: 10.1002/ajoc.202000675

Water-Dependent Selective Synthesis of Mono- or Bis-Selanyl Alkenes from Terminal Alkynes

Eduardo Q. Luz, Eric F. Lopes, Vanessa G. Ricordi, Claudio Santi, Thiago Barcellos, Eder J. Lenardão, Gelson Perin and Diego Alves

ChemistrySelect, 2016, 1, 4289
DOI: 10.1002/slct.201601177

Methylselenized Glucose: Improvement of the Stability of Glucose-Supported Selenium via the End-Capping Strategy

Qiyuan Wang, Peizi Li, Tao Li, Menglan Liu, Shimin Zuo, Jian Liu, Lin Xu, Xu Zhang and Lei Yu

Ind. Eng. Chem. Res., 2021, 60, 8659
DOI: 10.1021/acs.iecr.1c01437

Synthesis of Fully Functionalized 5‐Selanyl‐1,2,3‐triazoles: Copper‐Catalysed Three‐Component Reaction of Ethynylstibanes, Organic Azides, and Diaryl Diselenides

Mizuki Yamada, Mio Matsumura, Fumina Takino, Yuki Murata, Yuka Kurata, Masatoshi Kawahata, Kentaro Yamaguchi, Naoki Kakusawa and Shuji Yasuike

Eur J Org Chem, 2018, 2018, 170
DOI: 10.1002/ejoc.201701389

Perspective in Green Chemistry for Organoselenium Compounds (no more an oxymoron)

Claudio Santi

CGC, 2019, 6, 9
DOI: 10.2174/221334610601190329164654

Recent Advances on C-Se Bond-forming Reactions at Low and Room Temperature

Amol D. Sonawane and Mamoru Koketsu

COC, 2020, 23, 3206
DOI: 10.2174/1385272823666191209111934

N-doped and Se incorporated reduced graphene oxide nanocomposite as a new adsorbent for efficient Ni(II) ion removal from aqueous sample

Erum Asghar Ali, Khaled Elsaid, David James Hughes, Mohamed Mahmoud Nasef, Junaid Ali Syed, Mohsin Ali, Ahmed Abdel-Wahab, Khalid Ahmed and Zafar Khan Ghouri

emergent mater., 2024, 7, 1031
DOI: 10.1007/s42247-023-00608-7

Design and Synthesis of DiselenoBisBenzamides (DISeBAs) as Nucleocapsid Protein 7 (NCp7) Inhibitors with anti-HIV Activity

Luca Sancineto, Alice Mariotti, Luana Bagnoli, Francesca Marini, Jenny Desantis, Nunzio Iraci, Claudio Santi, Christophe Pannecouque and Oriana Tabarrini

J. Med. Chem., 2015, 58, 9601
DOI: 10.1021/acs.jmedchem.5b01183

Synthesis, photoluminescence, antimicrobial evaluation, molecular docking, and pharmacokinetic prediction of new pyrimidoselenolo[2,3-d]pyrimidine derivatives

Mahmoud S. Tolba, Mostafa Ahmed, Ahmed A.K. Mohammed, Abdelreheem Abdelfatah Saddik, Mostafa Sayed, Reda Hassanien, Adel M. Kamal El-Dean, Abdelfattah Hassan and Osama Younis

Journal of Molecular Structure, 2025, 1336, 142097
DOI: 10.1016/j.molstruc.2025.142097

Organocatalysed Synthesis of Selenium Containing Scaffolds

Amol D. Sonawane and Mamoru Koketsu

COCAT, 2021, 8, 5
DOI: 10.2174/2213337207999200414143605

Synthesis of organoselenium compounds using electrochemical and photochemical methods as novel approaches in organic chemistry

Adrián A. Heredia, Lydia M. Bouchet, Willber D. Castro-Godoy and Juan E. Argüello

Tetrahedron, 2023, 148, 133667
DOI: 10.1016/j.tet.2023.133667

Synergistic Catalysis of Se and Cu for the Activation of α‐H of Methyl Ketones with Molecular Oxygen/Alcohol to Produce α‐Keto Acetals†

Chao Chen, Zhicheng Cao, Xu Zhang, Yiming Li, Lei Yu and Xuefeng Jiang

Chin. J. Chem., 2020, 38, 1045
DOI: 10.1002/cjoc.202000089

Catalyst-free selenylation of acylacetylenes with secondary phosphine selenides and water: A short-cut to bis(2-acylvinyl) selenides

Pavel A. Volkov, Nina K. Gusarova, Kseniya O. Khrapova, Anton A. Telezhkin, Nina I. Ivanova, Alexander I. Albanov and Boris A. Trofimov

Journal of Organometallic Chemistry, 2018, 867, 79
DOI: 10.1016/j.jorganchem.2017.09.031

Selenium Dioxide Mediated Benzylic sp3 C-H Oxidation in Acetic Acid: Synthesis of Lophine Derivatives from α-Methylene Ketones via a Domino Multicomponent Reaction

Vineet Jeena and Mncedisi Mazibuko

HETEROCYCLES, 2017, 94, 1909
DOI: 10.3987/COM-17-13769

Reaction of Acyl Chlorides withIn SituFormed Zinc Selenolates: Synthesis of SelenoestersversusRing-Opening Reaction of Tetrahydrofuran

Gemma Bellino, Marialaura Scisciani, Jaqueline Pinto Vargas, Luca Sancineto, Luana Bagnoli, Francesca Marini, Diogo Seibert Lüdtke, Eder Joao Lenardao and Claudio Santi

Journal of Chemistry, 2016, 2016, 1
DOI: 10.1155/2016/2849140

Selective Synthesis of Vinyl‐ or Alkynyl Chalcogenides from Glycerol and their Water‐Soluble Derivatives

Liane K. Soares, Rafaela B. Silva, Thiago J. Peglow, Márcio S. Silva, Raquel G. Jacob, Diego Alves and Gelson Perin

ChemistrySelect, 2016, 1, 2009
DOI: 10.1002/slct.201600338

A Straightforward Access to Stable β‐Functionalized Alkyl Selenols

Damiano Tanini, Caterina Tiberi, Cristina Gellini, Pier Remigio Salvi and Antonella Capperucci

Adv Synth Catal, 2018, 360, 3367
DOI: 10.1002/adsc.201800602

Reaction of Selenyl Chlorides with β-Diketones

I. V. Svistunova, G. O. Tretyakova and Z. N. Puzyrkov

Russ J Gen Chem, 2022, 92, 977
DOI: 10.1134/S1070363222060093

Development of a General Synthetic Method for Organoselenium Compounds Utilizing Copper Catalyzed Cross Coupling and C-H Bond Activation

Mio Matsumura

YAKUGAKU ZASSHI, 2020, 140, 1101
DOI: 10.1248/yakushi.20-00112

Recent Advances in Microwave‐assisted Cross‐Coupling Reactions

Matiur Rahman, Sumit Ghosh, Dhananjay Bhattacherjee, Grigory V. Zyryanov, Avik Kumar Bagdi and Alakananda Hajra

Asian J Org Chem, 2022, 11
DOI: 10.1002/ajoc.202200179

Copper Catalysis and Organocatalysis Showing the Way: Synthesis of Selenium‐Containing Highly Functionalized 1,2,3‐Triazoles

Diego Alves, Bruna Goldani, Eder J. Lenardão, Gelson Perin, Ricardo F. Schumacher and Márcio W. Paixão

The Chemical Record, 2018, 18, 527
DOI: 10.1002/tcr.201700058

Bisarylselanylbenzo‐2,1,3‐selenadiazoles: Synthesis, Photophysical, Electrochemical and Singlet‐Oxygen‐Generation Properties

Renata A. Balaguez, Roberta Krüger, Bruna Iepsen, Ricardo F. Schumacher, Robson S. Oliboni, Thiago Barcellos, Helena C. Junqueira, Maurício S. Baptista, Bernardo A. Iglesias and Diego Alves

Eur J Org Chem, 2018, 2018, 6507
DOI: 10.1002/ejoc.201801186

Reaction of bis[(2-chlorocarbonyl)phenyl] Diselenide with Phenols, Aminophenols, and Other Amines towards Diphenyl Diselenides with Antimicrobial and Antiviral Properties

Mirosław Giurg, Anna Gołąb, Jakub Suchodolski, Rafał Kaleta, Anna Krasowska, Egbert Piasecki and Magdalena Piętka-Ottlik

Molecules, 2017, 22, 974
DOI: 10.3390/molecules22060974

Design and Preparation of Polymer Resin‐Supported Proline Catalyst with Industrial Application Potential

Mr. Lin Xu , Mr. Jiejun Huang , Ming Zhang, Lei Yu and Yining Fan

ChemistrySelect, 2016, 1, 1933
DOI: 10.1002/slct.201600404

2-Bromomethyl-1,3-thiaselenole in click chemistry: Synthesis of 1-(2,3-dihydro-1,4-thiaselenin-2-yl)-1H-1,2,3-triazoles via copper-catalyzed and thermal 1,3-dipolar cycloaddition with alkynes

Svetlana V. Amosova, Alexander V. Martynov and Vladimir A. Potapov

Journal of Organometallic Chemistry, 2022, 977, 122442
DOI: 10.1016/j.jorganchem.2022.122442

Green solvents in organoselenium chemistry

Marina D. Kostić and Vera M. Divac

Environ Chem Lett, 2019, 17, 897
DOI: 10.1007/s10311-018-00848-8

Easily fabricated Fe/Se soft magnetic material for catalytic phenol oxidation

Zhida Zhu, Shuai Sun, Shuai Tang, Sainan Chu and Xu Zhang

Molecular Catalysis, 2021, 515, 111923
DOI: 10.1016/j.mcat.2021.111923

Transition‐Metal‐Free C−S, C−Se, and C−Te Bond Formation from Organoboron Compounds

Manoela Sacramento, Gabriel P. Costa, Angelita M. Barcellos, Gelson Perin, Eder J. Lenardão and Diego Alves

The Chemical Record, 2021, 21, 2855
DOI: 10.1002/tcr.202100021

Bis-triazolylchalcogenium-Functionalized Benzothiadiazole Derivatives as Light-up Sensors for DNA and BSA

Roberta Krüger, Allya Larroza, Mariana G. Fronza, Isadora Tisoco, Lucielli Savegnago, Joel S. Reis, Davi F. Back, Bernardo A. Iglesias and Diego Alves

J. Org. Chem., 2021, 86, 17866
DOI: 10.1021/acs.joc.1c02153

Antioxidant activity of selenenamide-based mimic as a function of the aromatic thiols nucleophilicity, a DFT-SAPE model

Ramesh Kheirabadi and Mohammad Izadyar

Computational Biology and Chemistry, 2018, 75, 213
DOI: 10.1016/j.compbiolchem.2018.05.017

Iron(III)-catalyzed synthesis of selenoesters from α-amino carbonyl derivatives at room temperature

Rana Chatterjee, Anindita Mukherjee, Sougata Santra, Grigory V. Zyryanov and Adinath Majee

Tetrahedron, 2019, 75, 130624
DOI: 10.1016/j.tet.2019.130624

Visible light-promoted, iodine-catalyzed selenoalkoxylation of olefins with diselenides and alcohols in the presence of hydrogen peroxide/air oxidant: an efficient access to α-alkoxyl selenides

Mingxuan Liu, Yiming Li, Lei Yu, Qing Xu and Xuefeng Jiang

Sci. China Chem., 2018, 61, 294
DOI: 10.1007/s11426-017-9158-y

Ag/Se‐Catalyzed Selective Epoxidation of β‐Ionone with Molecular Oxygen

Xu Zhang, Tingting Zuo and Lei Yu

ChemistrySelect, 2022, 7
DOI: 10.1002/slct.202203514

Green and Practical Oxidative Deoximation of Oximes to Ketones or Aldehydes with Hydrogen Peroxide/Air by Organoselenium Catalysis

Xiaobi Jing, Dandan Yuan and Lei Yu

Adv Synth Catal, 2017, 359, 1194
DOI: 10.1002/adsc.201601353

Investigation of production mechanism, structure, and formulation of Se-methyl methaneselenoate and its halogen derivatives by density functional theory (DFT)

Fateme Fallah Irsafli, Leila Mahdavian and Azam Marjani

Computational and Theoretical Chemistry, 2023, 1230, 114376
DOI: 10.1016/j.comptc.2023.114376

Ultrasound-promoted organocatalytic enamine–azide [3 + 2] cycloaddition reactions for the synthesis of ((arylselanyl)phenyl-1H-1,2,3-triazol-4-yl)ketones

Gabriel P Costa, Natália Seus, Juliano A Roehrs, Raquel G Jacob, Ricardo F Schumacher, Thiago Barcellos, Rafael Luque and Diego Alves

Beilstein J. Org. Chem., 2017, 13, 694
DOI: 10.3762/bjoc.13.68

Simple and efficient copper-catalyzed synthesis of symmetrical diaryl selenides from triarylbismuthanes and selenium under aerobic conditions

Mio Matsumura, Hanae Kumagai, Yuki Murata, Naoki Kakusawa and Shuji Yasuike

Journal of Organometallic Chemistry, 2016, 807, 11
DOI: 10.1016/j.jorganchem.2016.02.006

Selenium-Catalyzed Reduction of Hydroperoxides in Chemistry and Biology

Laura Orian and Leopold Flohé

Antioxidants, 2021, 10, 1560
DOI: 10.3390/antiox10101560

Exploring the Role of Substitution on the Formation of Se···O/N Noncovalent Bonds

Rahul Shukla and Deepak Chopra

J. Phys. Chem. B, 2015, 119, 14857
DOI: 10.1021/acs.jpcb.5b08684

Contrasting Reactivity of 2‐chloro‐1‐formyl‐3‐hydroxymethylenecyclohexene and its Schiff Bases towards Disodium Diselenide: Isolation of Selenospirocycles versus Azapentalenes

Krishnan Venkateshwaran, Poonam Rajesh Prasad, Rajesh Deka, Saravanan Raju, Harkesh B. Singh and Ray J. Butcher

Asian J Org Chem, 2019, 8, 128
DOI: 10.1002/ajoc.201800544

Alkynylselenium-functionalized benzothiadiazoles: Synthesis, photophysics, electrochemistry, and biomolecular interaction studies

Carolina H. Silveira, Mariana G. Fronza, Renata A. Balaguez, Allya M.E. Larroza, Lucielli Savegnago, Davi F. Back, Bernardo A. Iglesias and Diego Alves

Dyes and Pigments, 2021, 185, 108910
DOI: 10.1016/j.dyepig.2020.108910

Continuous Bioinspired Oxidation of Sulfides

Francesca Mangiavacchi, Letizia Crociani, Luca Sancineto, Francesca Marini and Claudio Santi

Molecules, 2020, 25, 2711
DOI: 10.3390/molecules25112711

A Study on the Reactions of SeO2 with Pyrroles and N‐Substituted Indoles in Non‐Anhydrous Ethanol under Non‐Inert Atmosphere

Ranadeep Talukdar

Asian J Org Chem, 2019, 8, 88
DOI: 10.1002/ajoc.201800584

Unexpected Pd/C-catalyzed room temperature and atmospheric pressure hydrogenation of 2-methylenecyclobutanones

Yufan Yang, Mengxuan Li, Hongen Cao, Xu Zhang and Lei Yu

Molecular Catalysis, 2019, 474, 110450
DOI: 10.1016/j.mcat.2019.110450

Tuning the triplet population of arylselanyl-BODIPY photosensitizers through substituents engineering for triplet-triplet annihilation photon upconversion with perylene

Ryohei Hasegawa, Masato Ito and Yuji Kubo

J. Porphyrins Phthalocyanines, 2023, 27, 757
DOI: 10.1142/S1088424623500037

Reusable Selenenyl Iodide‐Initiated Cascade Cyclization of Polyenes with N‐terminating Groups

Satoru Kuwano, Jun Kikushima, Takaaki Nakada, Shohei Sase and Kei Goto

Chemistry An Asian Journal, 2025, 20
DOI: 10.1002/asia.202500347

Mechanistic Insight into the Oxidation of Organic Phenylselenides by H2O2

Giovanni Ribaudo, Massimo Bellanda, Ileana Menegazzo, Lando P. Wolters, Marco Bortoli, Gerardo Ferrer‐Sueta, Giuseppe Zagotto and Laura Orian

Chemistry A European J, 2017, 23, 2405
DOI: 10.1002/chem.201604915

Copper-catalyzed synthesis of 1,3,5-triaryl-4-(organylselanyl)-1H-pyrazoles by one-pot multicomponent reactions

Thalita F.B. de Aquino, Jessica P. Seidel, Daniela H. de Oliveira, José Edmilson R. do Nascimento, Diego Alves, Gelson Perin, Eder J. Lenardão, Ricardo F. Schumacher and Raquel G. Jacob

Tetrahedron Letters, 2018, 59, 4090
DOI: 10.1016/j.tetlet.2018.10.008

Energy saving and environment-friendly element-transfer reactions with industrial application potential

Chao Chen, Yitao Cao, Xixi Wu, Yuanli Cai, Jian Liu, Lin Xu, Kehong Ding and Lei Yu

Chinese Chemical Letters, 2020, 31, 1078
DOI: 10.1016/j.cclet.2019.12.019

Cu(II) and Ag(I) complexes of the pyrazole-derived diorganoselenide (pzCH2CH2)2Se. Synthesis, solid state structure and solution behavior

Roxana A. Popa, Vito Lippolis and Anca Silvestru

Inorganica Chimica Acta, 2021, 520, 120272
DOI: 10.1016/j.ica.2021.120272

Synthesis and evaluation of dihydropyrimidinone-derived selenoesters as multi-targeted directed compounds against Alzheimer’s disease

Flavio A.R. Barbosa, Rômulo F.S. Canto, Sumbal Saba, Jamal Rafique and Antonio L. Braga

Bioorganic & Medicinal Chemistry, 2016, 24, 5762
DOI: 10.1016/j.bmc.2016.09.031

Chiral Bifunctional Selenide Catalysts for Asymmetric Bromolactonization

Ryuichi Nishiyori, John R. J. Maynard and Seiji Shirakawa

Asian J Org Chem, 2020, 9, 192
DOI: 10.1002/ajoc.201900688

Water and Aqueous Mixtures as Convenient Alternative Media for Organoselenium Chemistry

Claudio Santi, Raquel Jacob, Bonifacio Monti, Luana Bagnoli, Luca Sancineto and Eder Lenardão

Molecules, 2016, 21, 1482
DOI: 10.3390/molecules21111482

Insights into the Recent Synthetic Advances of Organoselenium Compounds

Priyanka N. Makhal, Arijit Nandi and Venkata Rao Kaki

ChemistrySelect, 2021, 6, 663
DOI: 10.1002/slct.202004029