Retracted Article: Visible-light-induced oxidative difunctionalization of styrenes: synthesis of α-trifluoromethylthio-substituted ketones

2018 ◽  
Vol 54 (16) ◽  
pp. 1976-1979 ◽  
Author(s):  
Arvind Kumar Yadav ◽  
Krishna Nand Singh

Synthesis of α-trifluoromethylthio-substituted ketones has been accomplished through photoredox catalysis from easily accessible styrenes. The present approach involves the use of inexpensive eosin Y as an organophotoredox catalyst and a CF3SO2Na/CS2 blend as a new source of SCF3 radicals at room temperature.

Synlett ◽  
2020 ◽  
Vol 31 (04) ◽  
pp. 363-368 ◽  
Author(s):  
Can Jin ◽  
Bin Sun ◽  
Tengwei Xu ◽  
Liang Zhang ◽  
Rui Zhu ◽  
...  

A visible-light-induced direct C–H alkylation of imidazo[1,2-a]pyridines has been developed. It proceeds at room temperature by employing inexpensive Eosin Y as a photocatalyst and alkyl N-hydroxyphthalimide (NHP) esters as alkylation reagents. A variety of NHP esters derived from aliphatic carboxylic acids (primary, secondary, and tertiary) were tolerated in this protocol, giving the corresponding C-5-alkylated products in moderate to excellent yields. Mechanistic studies indicate that a radical decarboxylative coupling pathway was involved in this process.


2021 ◽  
Author(s):  
Hui Liu ◽  
Chao Liu ◽  
Shanyi Chen ◽  
Qihong Lai ◽  
Yulin Lin ◽  
...  

An efficient method for the direct oxidative lactonization of the C(sp3)–H bonds of benzyl via visible-light-induced photoredox catalysis. The metal-free protocol delivers diverse phthalides using O2 as the sole terminal oxidant at room temperature.


2018 ◽  
Vol 42 (9) ◽  
pp. 6617-6620 ◽  
Author(s):  
Shikha Singh ◽  
Parul Chauhan ◽  
Makthala Ravi ◽  
Prem P. Yadav

Synthesis of heterobiaryl-pyrazolo[3,4-b]pyridines via Lewis acid and visible light photo-catalysis at room temperature.


2020 ◽  
Vol 73 (3) ◽  
pp. 189
Author(s):  
Theerada Seehamongkol ◽  
Tyra H. Horngren ◽  
Mohammed A. M. Alhajji ◽  
Joshua Almond-Thynne ◽  
Milena L. Czyz ◽  
...  

A methodology for a radical Pictet–Spengler reaction promoted by visible light photoredox catalysis is described. This strategy furnishes tetrahydroisoquinoline derivatives bearing electron poor and electron rich substituents. The reaction proceeds at room temperature and with excellent regioselectivity for the 6-endo intramolecular cyclisation. This radical approach provides a complementary method for the synthesis of the tetrahydroisoquinoline scaffold with substitution patterns inaccessible via established thermal transformations.


ChemInform ◽  
2015 ◽  
Vol 46 (32) ◽  
pp. no-no
Author(s):  
Jun Xuan ◽  
Ting-Ting Zeng ◽  
Jia-Rong Chen ◽  
Liang-Qiu Lu ◽  
Wen-Jing Xiao

2018 ◽  
Vol 20 (6) ◽  
pp. 1233-1237 ◽  
Author(s):  
Mei-jie Bu ◽  
Chun Cai ◽  
Fabrice Gallou ◽  
Bruce H. Lipshutz

A new photocatalyst attached to the designer surfactant PQS has been developed that self-aggregates into micelles, thereby enabling photoredox catalysis conducted in water at room temperature without any additives or co-solvents.


ChemInform ◽  
2015 ◽  
Vol 46 (25) ◽  
pp. no-no
Author(s):  
Wei Guo ◽  
Liang-Qiu Lu ◽  
Yue Wang ◽  
Ya-Ni Wang ◽  
Jia-Rong Chen ◽  
...  

2014 ◽  
Vol 54 (7) ◽  
pp. 2265-2269 ◽  
Author(s):  
Wei Guo ◽  
Liang-Qiu Lu ◽  
Yue Wang ◽  
Ya-Ni Wang ◽  
Jia-Rong Chen ◽  
...  

2015 ◽  
Vol 21 (13) ◽  
pp. 4962-4965 ◽  
Author(s):  
Jun Xuan ◽  
Ting-Ting Zeng ◽  
Jia-Rong Chen ◽  
Liang-Qiu Lu ◽  
Wen-Jing Xiao

2014 ◽  
Vol 50 (18) ◽  
pp. 2308-2310 ◽  
Author(s):  
Pan Xu ◽  
Ablimit Abdukader ◽  
Kaidong Hu ◽  
Yixiang Cheng ◽  
Chengjian Zhu

A visible-light-induced decarboxylative trifluoromethylation of α,β-unsaturated carboxylic acids, which uses the Togni reagent as the CF3 source is disclosed.


Sign in / Sign up

Export Citation Format

Share Document