Catalytic, metal-free sulfonylcyanation of alkenes via visible light organophotoredox catalysis

2018 ◽  
Vol 54 (25) ◽  
pp. 3162-3165 ◽  
Author(s):  
Jianfeng Sun ◽  
Peng Li ◽  
Lei Guo ◽  
Fang Yu ◽  
Yu-Peng He ◽  
...  

A catalytic, redox-neutral group transfer radical addition of olefins with tosyl cyanide via visible light-induced organophotoredox catalysis has been described.

Synthesis ◽  
2020 ◽  
Vol 53 (01) ◽  
pp. 123-134
Author(s):  
Constantin Czekelius ◽  
Lucas Helmecke ◽  
Michael Spittler ◽  
Bernd M. Schmidt

A comparison of two catalytic, metal-free iodoperfluoro­alkylation protocols is presented. Frustrated Lewis pairs [ t Bu3P/B(C6F5)3] or phosphines/phosphites under visible light irradiation efficiently mediate the functionalization of non-activated alkenes and alkynes. A comprehensive account of the corresponding substrate scopes as well as insights into the mechanistic details of both reaction pathways are provided.


2019 ◽  
Vol 6 (13) ◽  
pp. 2245-2249 ◽  
Author(s):  
Guibing Wu ◽  
Jingwen Wang ◽  
Chengyu Liu ◽  
Maolin Sun ◽  
Lei Zhang ◽  
...  

A metal-free photoredox catalyzed decarboxylative radical coupling of free-carboxylic acids and glyoxylic oximes was developed to synthesize α,β-diamino acids.


2017 ◽  
Vol 19 (13) ◽  
pp. 2941-2944 ◽  
Author(s):  
Ya Ding ◽  
Wenkai Zhang ◽  
Hao Li ◽  
Yunge Meng ◽  
Te Zhang ◽  
...  

A green and cost-effective method has been developed for the conversion of alkenes to ketones under metal-free conditions.


2021 ◽  
Vol 23 (4) ◽  
pp. 1638-1641
Author(s):  
Pannan Miao ◽  
Ruining Li ◽  
Xianfeng Lin ◽  
Liangming Rao ◽  
Zhankui Sun

Through a relay olefination and radical addition process, we developed cascade Wittig/hydroalkylation reactions induced by visible light. This metal-free radical approach features mild conditions, robustness, and excellent functionality tolerance.


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.


ChemCatChem ◽  
2019 ◽  
Vol 11 (14) ◽  
pp. 3307-3317
Author(s):  
Andreea L. Chibac ◽  
Violeta Melinte ◽  
Vlasta Brezová ◽  
Estelle Renard ◽  
Arnaud Brosseau ◽  
...  

2021 ◽  
Vol 19 (16) ◽  
pp. 3735-3742
Author(s):  
Se Hyun Kim ◽  
Ju Hyeon An ◽  
Jun Hee Lee

Here, we provide an operationally simple protocol for the highly chemoselective deoxygenation of various functionalized N-heterocyclic N-oxides under visible light-mediated photoredox conditions with Na2-eosin Y as an organophotocatalyst.


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