Electrochemical difunctionalization of alkenes and alkynes for the synthesis of organochalcogens involving C–S/Se bond formation

Literature Information

Publication Date 2023-11-23
DOI 10.1039/D3QO01844J
Impact Factor 5.281
Authors

Jianchao Liu, Jie-Ping Wan, Yunyun Liu


View Original

Abstract

Organochalcogen compounds containing C–S/Se bond are motifs frequently found in various natural products, bioactive compounds, as well as functional materials. On the other hand, electrochemical organic synthesis has been regarded as a green and sustainable technology in which electrons serve as redox reagents. Given the wide presence of alkenes and alkynes as substrates, the electrochemical difunctionalization of alkenes and alkynes involving C–S/Se bond formation with high step-economy has recently attracted much attention from synthetic organic chemists. This review is devoted to highlighting the latest achievements in the development of the electrochemical difunctionalization of alkenes and alkynes for the synthesis of organochalcogens, including the oxychalcogenation, carbochalcogenation, aminochalcogenation, halochalcogenation, and dichalcogenation of alkenes and alkynes from 2018 to 2023.

Related Literature

Aromaticity in all-metal annular systems: the counter-ion effect

Arindam Chakraborty, Santanab Giri, Soma Duley, Anakuthil Anoop, Patrick Bultinck, Pratim K. Chattaraj

2011-07-26 Perspective

DOI: 10.1039/C1CP21430F

Graphical prediction of quantum interference-induced transmission nodes in functionalized organic molecules

Troels Markussen, Robert Stadler, Kristian S. Thygesen

2011-06-28 Paper

DOI: 10.1039/C1CP20924H

A layered structure at the surface of P3HT/PCBM blends

Natalya Schmerl, Gunther Andersson

2011-07-18 Paper

DOI: 10.1039/C1CP20734B

A new approach to local hardness

T. Gál, P. Geerlings, F. De Proft, M. Torrent-Sucarrat

2011-07-26 Paper

DOI: 10.1039/C1CP21213C

π-Stacking between Casiopeinas® and DNA bases

Rodrigo Galindo-Murillo, Joseelyne Hernandez-Lima, Mayra González-Rendón, Lena Ruíz-Azuara, Rafael Moreno-Esparza

2011-07-12 Paper

DOI: 10.1039/C1CP20183B

Platinum-nanogaps for single-molecule electronics: room-temperature stability

Ferry Prins, Ahson J. Shaikh, Jan H. van Esch, Rienk Eelkema, Herre S. J. van der Zant

2011-05-09 Paper

DOI: 10.1039/C1CP20555B

Intramolecular charge transfer and dual fluorescence of 4-(dimethylamino)benzonitrile: ultrafast branching followed by a two-fold decay mechanism‡

Pedro B. Coto, Luis Serrano-Andrés, Thomas Gustavsson, Takashige Fujiwara, Edward C. Lim

2011-07-18 Paper

DOI: 10.1039/C1CP21089K

Towards the computational modelling of polyoxoanions on metal surfaces: IR spectrum characterisation of [SiW12O40]4− on Ag(111)

Xavier Aparicio-Anglès, Anna Clotet, Josep M. Poblet

2011-07-11 Paper

DOI: 10.1039/C0CP02602F

Spin seebeck coefficient of a molecular spin pump

Jonas Fransson, Michael Galperin

2011-06-07 Paper

DOI: 10.1039/C1CP20720B

You might also like

Compound Q&A

How should 2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) be stored?

2-Methylbenzene-1,4-diamine dihydrochloride (CAS: 615-45-2) should be stored in ...

615-45-22-Methylbenzene-1,4-...
Compound Q&A

Is (1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide (CAS: 132747-20-7) safe?

(1S,4S)-2,5-Diazabicyclo[2.2.1]heptane dihydrobromide is generally considered sa...

132747-20-7(1S,4S)-2,5-Diazabic...
Compound Q&A

What industries use (6-Chloropyridazin-3-YL)methanamine (CAS: 871826-15-2)?

(6-Chloropyridazin-3-YL)methanamine finds applications in the pharmaceutical ind...

871826-15-2(6-Chloropyridazin-3...
Compound Q&A

What are the main uses of 2-Fluoro-3-methylphenol (CAS: 77772-72-6)?

2-Fluoro-3-methylphenol is primarily used in the synthesis of pharmaceuticals, p...

77772-72-62-Fluoro-3-methylphe...
Compound Q&A

What precautions should be taken when handling 3-Methoxy-4-nitrobenzonitrile (CAS: 177476-75-4)?

When handling 3-Methoxy-4-nitrobenzonitrile, it is important to wear appropriate...

177476-75-43-Methoxy-4-nitroben...
Compound Q&A

What precautions should be taken when handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4)?

When handling 1,3-Oxazolo[4,5-b]pyridine-2(3H)-thione (CAS: 211949-57-4), it is ...

211949-57-4[1,3]Oxazolo[4,5-b]p...
Compound Q&A

What regulatory guidelines apply to 4-Ethynylbenzamide (CAS: 90347-86-7)?

4-Ethynylbenzamide (CAS: 90347-86-7) falls under various regulatory guidelines i...

90347-86-74-Ethynylbenzamide
Compound Q&A

What are the main uses of 3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone (CAS: 186822-57-1)?

3-(2-Ethylphenyl)-2-thioxo-4-imidazolidinone is primarily used as an intermediat...

186822-57-13-(2-Ethylphenyl)-2-...
Compound Q&A

What is (2-Fluoro-6-methoxyphenyl)acetic acid (CAS: 500912-19-6)?

(2-Fluoro-6-methoxyphenyl)acetic acid, also known as 4-fluoro-3-methoxybenzoic a...

500912-19-6(2-Fluoro-6-methoxyp...
Compound Q&A

What is the market or research trend for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9)?

Market trends for 2-[4-(Hydroxymethyl)phenoxy]ethanol (CAS: 102196-18-9) indicat...

102196-18-92-[4-(Hydroxymethyl)...

Source Journal

Organic Chemistry Frontiers

Organic Chemistry Frontiers
CiteScore: 7.8
Self-citation Rate: 8.7%
Articles per Year: 724

Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.