Correction to “A New Approach to Nitrones through Cascade Reaction of Nitro Compounds Enabled by Visible Light Photoredox Catalysis”

2015 ◽  
Vol 17 (13) ◽  
pp. 3378-3378
Author(s):  
Cheng-Wei Lin ◽  
Bor-Cherng Hong ◽  
Wan-Chen Chang ◽  
Gene-Hsiang Lee
ChemInform ◽  
2015 ◽  
Vol 46 (38) ◽  
pp. no-no
Author(s):  
Cheng-Wei Lin ◽  
Bor-Cherng Hong ◽  
Wan-Chen Chang ◽  
Gene-Hsiang Lee

2015 ◽  
Vol 17 (10) ◽  
pp. 2314-2317 ◽  
Author(s):  
Cheng-Wei Lin ◽  
Bor-Cherng Hong ◽  
Wan-Chen Chang ◽  
Gene-Hsiang Lee

2013 ◽  
Vol 15 (11) ◽  
pp. 2660-2663 ◽  
Author(s):  
Shunyou Cai ◽  
Shaolong Zhang ◽  
Yaohong Zhao ◽  
David Zhigang Wang

ChemInform ◽  
2013 ◽  
Vol 44 (38) ◽  
pp. no-no
Author(s):  
Shunyou Cai ◽  
Shaolong Zhang ◽  
Yaohong Zhao ◽  
Zhigang Wang

2018 ◽  
Vol 16 (3) ◽  
pp. 414-423 ◽  
Author(s):  
Xu Liu ◽  
Zhongjie Wu ◽  
Zeguo Zhang ◽  
Ping Liu ◽  
Peipei Sun

In the presence of Ru(phen)3Cl2 or fac-Ir(ppy)3 under visible-light irradiation, the addition of fluorinated radicals to N-arylacrylamides followed by an intramolecular cyano group insertion cascade cyclization process produced the target compounds in moderate to good yields.


2016 ◽  
Vol 81 (20) ◽  
pp. 9992-10001 ◽  
Author(s):  
Jin Li ◽  
Jingzhi Chen ◽  
Wei Jiao ◽  
Guoqiang Wang ◽  
Ying Li ◽  
...  

Author(s):  
Arumugavel Murugan ◽  
Venkata Nagarjuna Babu ◽  
Nagaraj Sabarinathan ◽  
Sharada Duddu. S

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.


Synthesis ◽  
2020 ◽  
Author(s):  
Jia-Jia Zhao ◽  
Hong-Hao Zhang ◽  
Shouyun Yu

Visible light photoredox catalysis has recently emerged as a powerful tool for the development of new and valuable chemical transformations under mild conditions. Visible-light promoted enantioselective radical transformations of imines and iminium intermediates provide new opportunities for the asymmetric synthesis of amines and asymmetric β-functionalization of unsaturated carbonyl compounds. In this review, the advance in the catalytic asymmetric radical functionalization of imines, as well as iminium intermediates, are summarized. 1 Introduction 2 The enantioselective radical functionalization of imines 2.1 Asymmetric reduction 2.2 Asymmetric cyclization 2.3 Asymmetric addition 2.4 Asymmetric radical coupling 3 The enantioselective radical functionalization of iminium ions 3.1 Asymmetric radical alkylation 3.2 Asymmetric radical acylation 4 Conclusion


2013 ◽  
Vol 15 (9) ◽  
pp. 2136-2139 ◽  
Author(s):  
Yusuke Yasu ◽  
Takashi Koike ◽  
Munetaka Akita

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