Benzylic C(sp3)–H Functionalization for C–N and C–O Bond Formation via Visible Light Photoredox Catalysis

2016 ◽  
Vol 81 (16) ◽  
pp. 7161-7171 ◽  
Author(s):  
Ganesh Pandey ◽  
Ramkrishna Laha ◽  
Deepak Singh
Keyword(s):  
Visible Light ◽  
Bond Formation ◽  
Photoredox Catalysis

Visible light photocatalysis in synthesis of pharmaceutically relevant heterocyclic scaffolds

2022 ◽  
Author(s):  
Vishal Srivastava ◽  
Pravin Kumar Singh ◽  
Shraddha Tivari ◽  
Praveen Pratap Singh
Keyword(s):  
Natural Products ◽  
Visible Light ◽  
Chemical Bond ◽  
Organic Synthesis ◽  
Bond Formation ◽  
Visible Light Photocatalysis ◽  
Photoredox Catalysis ◽  
Chemical Bond Formation

Visible light and photoredox catalysis have emerged as a powerful and long-lasting tool for organic synthesis, demonstrating the importance of a variety of chemical bond formation methods. Natural products, physiologically...

ChemInform Abstract: Room Temperature C-P Bond Formation Enabled by Merging Nickel Catalysis and Visible-Light-Induced Photoredox Catalysis.

ChemInform ◽  
2015 ◽  
Vol 46 (32) ◽  
pp. no-no
Author(s):  
Jun Xuan ◽  
Ting-Ting Zeng ◽  
Jia-Rong Chen ◽  
Liang-Qiu Lu ◽  
Wen-Jing Xiao
Keyword(s):  
Visible Light ◽  
Room Temperature ◽  
Bond Formation ◽  
Nickel Catalysis ◽  
Photoredox Catalysis

Metal-free desilylative C–C bond formation by visible-light photoredox catalysis

2019 ◽  
Vol 55 (20) ◽  
pp. 2980-2983 ◽  
Author(s):  
Mustafa Uygur ◽  
Tobias Danelzik ◽  
Olga García Mancheño
Keyword(s):  
Visible Light ◽  
Bond Formation ◽  
Photoredox Catalysis ◽  
Metal Free

A novel metal-free desilylative C–C bond formation from simple organosilanes by visible-light acridinium photoredox catalysis is presented.

Room Temperature CP Bond Formation Enabled by Merging Nickel Catalysis and Visible-Light-Induced Photoredox Catalysis

2015 ◽  
Vol 21 (13) ◽  
pp. 4962-4965 ◽  
Author(s):  
Jun Xuan ◽  
Ting-Ting Zeng ◽  
Jia-Rong Chen ◽  
Liang-Qiu Lu ◽  
Wen-Jing Xiao
Keyword(s):  
Visible Light ◽  
Room Temperature ◽  
Bond Formation ◽  
Nickel Catalysis ◽  
Photoredox Catalysis

scholarly journals Recent Advances in C-F Bond Cleavage Enabled by Visible Light Photoredox Catalysis

Molecules ◽  
2021 ◽  
Vol 26 (22) ◽  
pp. 7051
Author(s):  
Lei Zhou
Keyword(s):  
Visible Light ◽  
Future Development ◽  
Bond Cleavage ◽  
Bond Formation ◽  
Environmentally Benign ◽  
Personal Perspective ◽  
Photoredox Catalysis ◽  
Recent Advances ◽  
The Future ◽  
The Creation

The creation of new bonds via C-F bond cleavage of readily available per- or oligofluorinated compounds has received growing interest. Using such a strategy, a myriad of valuable partially fluorinated products can be prepared, which otherwise are difficult to make by the conventional C-F bond formation methods. Visible light photoredox catalysis has been proven as an important and powerful tool for defluorinative reactions due to its mild, easy to handle, and environmentally benign characteristics. Compared to the classical C-F activation that proceeds via two-electron processes, radicals are the key intermediates using visible light photoredox catalysis, providing new modes for the cleavage of C-F bonds. In this review, a summary of the visible light-promoted C-F bond cleavage since 2018 was presented. The contents were classified by the fluorosubstrates, including polyfluorinated arenes, gem-difluoroalkenes, trifluoromethyl arenes, and trifluoromethyl alkenes. An emphasis is placed on the discussion of the mechanisms and limitations of these reactions. Finally, my personal perspective on the future development of this rapidly emerging field was provided.

Remote C–C bond formation via visible light photoredox-catalyzed intramolecular hydrogen atom transfer

2020 ◽  
Vol 18 (24) ◽  
pp. 4519-4532 ◽  
Author(s):  
Hui Chen ◽  
Shouyun Yu
Keyword(s):  
Hydrogen Atom ◽  
Visible Light ◽  
Bond Formation ◽  
Hydrogen Atom Transfer ◽  
Atom Transfer ◽  
Photoredox Catalysis ◽  
Recent Advances ◽  
Intramolecular Hydrogen

Visible light photoredox catalysis combined with intramolecular hydrogen atom transfer (HAT) can serve as a unique tool for achieving remote C–C bond formation. Recent advances in photoredox-catalyzed remote C–C bond formation are summarized.

Visible light photoredox catalysis: conversion of a mixture of thiophenols and nitriles into 2-substituted benzothiazoles via consecutive C–S and C–N bond formation reactions

2018 ◽  
Vol 5 (9) ◽  
pp. 1527-1531 ◽  
Author(s):  
Palani Natarajan ◽  
Manjeet Manjeet ◽  
Muskan Muskan ◽  
Navpreet Kaur Brar ◽  
Jaskamal Jot Kaur
Keyword(s):  
Visible Light ◽  
Bond Formation ◽  
Eosin Y ◽  
Photoredox Catalysis ◽  
Alkyl Aryl ◽  
Air Atmosphere ◽  
Aryl Nitriles ◽  
Bond Formation Reactions

A novel, visible-light-mediated method for the synthesis of 2-substituted benzothiazoles from thiophenols and alkyl/aryl nitriles in the presence of eosin Y under air atmosphere is disclosed.

Oxy-Sulfonylation of Terminal Alkynes via C-S Coupling Enabled by Copper Photoredox Catalysis

2021 ◽  
Author(s):  
V. kishore Kumar Pampana ◽  
Vaibhav Pramod Charpe ◽  
Arunachalam Sagadevan ◽  
Deb Kumar Das ◽  
Chun-Cheng Lin ◽  
...  
Keyword(s):  
Visible Light ◽  
Bond Formation ◽  
Terminal Alkynes ◽  
Photoredox Catalysis ◽  
Trimethylsilyl Azide

We report the first literature example using visible light-induced trimethylsilyl azide (TMSN3)-assisted copper-catalyzed oxy-sulfonylation of terminal C≡C bond to form β-keto sulfones (C-S bond formation). TMS-N3 promotes the reaction by...

Regioselective C3-H Trifluoromethylation of 2H-Indazole Under Transition-Metal-Free Photoredox Catalysis

2019 ◽  
Author(s):  
Arumugavel Murugan ◽  
Venkata Nagarjuna Babu ◽  
Nagaraj Sabarinathan ◽  
Sharada Duddu. S
Keyword(s):  
Transition Metal ◽  
Visible Light ◽  
Practical Approach ◽  
Hypervalent Iodine ◽  
Radical Mechanism ◽  
Photoredox Catalysis ◽  
Metal Free

Here we report a visible-light-promoted metal-free regioselective C3-H trifluoromehtylation reaction that proceeds via radical mechanism and which supported by control experiments. The combination of photoredox catalysis and hypervalent iodine reagent provides a practical approach for the present trifluoromethylation reaction and synthesis of a library of trifluoromethylated indazoles.

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