Advanced search
Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 51, 2021 - Issue 5
Submit an article Journal homepage
341
Views
8
CrossRef citations to date
0
Altmetric
Articles

Photocatalyst-free photoredox synthesis of diaryl selenides by reaction of diselenides with aryldiazo sulfones

Jihoon JangDepartment of Chemistry, Soonchunhyang University, Asan, Chungnam, Republic of KoreaView further author information
,
Rabin KimDepartment of Chemistry, Soonchunhyang University, Asan, Chungnam, Republic of KoreaView further author information
&
Dae Young KimDepartment of Chemistry, Soonchunhyang University, Asan, Chungnam, Republic of KoreaCorrespondence[email protected]
View further author information
Pages 720-726 | Received 16 Oct 2020, Published online: 26 Nov 2020

Citations (8)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (1)

Saade Abdalkareem Jasim, Reena Solanki, Yaser Mohamed Hasan, Forat H. Alsultany, Zuhair I. Al Mashhadani & Zahra Moghadasi. (2024) An Interesting and Highly Efficient Route to 2-(Arylethynyl)Selanyl-Azoles: Fe3O4-Serine-CuI Nanocomposite Catalyzed Three-Component Coupling Reaction of Azoles, Se Powder, and Alkynes. Polycyclic Aromatic Compounds 44:2, pages 930-946.
Read now

Articles from other publishers (7)

Peng Hu, Weina Li, Yanmei Li, Yongxiang Su, Benshang Zhang & Li Shen. (2023) Synthesis of Benzoselenazoles Catalyzed by Copper(I) Complex Supported on Magnetic Nanoparticles. Catalysis Letters 154:5, pages 2396-2413.
Crossref
Felipe C. Braga, Guilherme M. Martins, Marcelo S. Franco, Luiz P. A. Belli, Kleber T. de Oliveira & Francisco F. de Assis. (2024) Catalyst-free photoarylation reactions promoted by visible light. Organic Chemistry Frontiers 11:4, pages 1251-1275.
Crossref
Ruchi Chawla, Atul K. Singh & Pradip K. Dutta. (2024) Arylazo sulfones: multifaceted photochemical reagents and beyond. Organic & Biomolecular Chemistry 22:5, pages 869-893.
Crossref
Adrián A. Heredia, Lydia M. Bouchet, Willber D. Castro-Godoy & Juan E. Argüello. (2023) Synthesis of organoselenium compounds using electrochemical and photochemical methods as novel approaches in organic chemistry. Tetrahedron 148, pages 133667.
Crossref
Stefano Protti & Maurizio Fagnoni. (2022) Recent Advances in Light-Induced Selenylation. ACS Organic & Inorganic Au 2:6, pages 455-463.
Crossref
Ruizhe Wang, Xinyu Wang, Shuai Mao, Yahao Zhao, Bo Yuan, Xue‐Yan Yang, Jianjun Li & Zhengkai Chen. (2022) Metal‐Free Photochemical C−Se Cross‐Coupling of Aryl Halides with Diselenides. Advanced Synthesis & Catalysis 364:9, pages 1607-1612.
Crossref
Juliano B. Azeredo, Filipe Penteado, Vanessa Nascimento, Luca Sancineto, Antonio L. Braga, Eder João Lenardao & Claudio Santi. (2022) “Green Is the Color”: An Update on Ecofriendly Aspects of Organoselenium Chemistry. Molecules 27:5, pages 1597.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.