Visible-light promoted γ-cyanoalkyl radical generation: three-component cyanopropylation/etherification of unactivated alkenes

2017 ◽  
Vol 53 (84) ◽  
pp. 11544-11547 ◽  
Author(s):  
Linyong Li ◽  
Haoguo Chen ◽  
Mingjing Mei ◽  
Lei Zhou

A photoredox approach to generate distal cyano-substituted alkyl radicals through C–C bond cleavage of cyclobutanone oximes was developed.

2019 ◽  
Author(s):  
Tuhin Patra ◽  
Satobhisha Mukherjee ◽  
Jiajia Ma ◽  
Felix Strieth-Kalthoff ◽  
Frank Glorius

<sub>A general strategy to access both aryl and alkyl radicals by photosensitized decarboxylation of the corresponding carboxylic acids esters has been developed. An energy transfer mediated homolysis of unsymmetrical sigma-bonds for a concerted fragmentation/decarboxylation process is involved. As a result, an independent aryl/alkyl radical generation step enables a series of key C-X and C-C bond forming reactions by simply changing the radical trapping agent.</sub>


2019 ◽  
Author(s):  
Frank Glorius ◽  
Tuhin Patra ◽  
Satobhisha Mukherjee ◽  
Jiajia Ma ◽  
Felix Strieth-Kalthoff

<sub>A general strategy to access both aryl and alkyl radicals by photosensitized decarboxylation of the corresponding carboxylic acids esters has been developed. An energy transfer mediated homolysis of unsymmetrical sigma-bonds for a concerted fragmentation/decarboxylation process is involved. As a result, an independent aryl/alkyl radical generation step enables a series of key C-X and C-C bond forming reactions by simply changing the radical trapping agent.</sub>


2019 ◽  
Author(s):  
Frank Glorius ◽  
Tuhin Patra ◽  
Satobhisha Mukherjee ◽  
Jiajia Ma ◽  
Felix Strieth-Kalthoff

<sub>A general strategy to access both aryl and alkyl radicals by photosensitized decarboxylation of the corresponding carboxylic acids esters has been developed. An energy transfer mediated homolysis of unsymmetrical sigma-bonds for a concerted fragmentation/decarboxylation process is involved. As a result, an independent aryl/alkyl radical generation step enables a series of key C-X and C-C bond forming reactions by simply changing the radical trapping agent.</sub>


2018 ◽  
Vol 54 (48) ◽  
pp. 6105-6112 ◽  
Author(s):  
Kunfang Jia ◽  
Yiyun Chen

The recent advancements in inert C(sp3)–H, C(sp3)–C(sp3), and C(sp3)–X bond cleavage/functionalization by visible-light-induced alkoxyl radical generation are discussed.


2017 ◽  
Vol 8 ◽  
pp. 1863-1877 ◽  
Author(s):  
Rashanique D Quarels ◽  
Xianglin Zhai ◽  
Neepa Kuruppu ◽  
Jenny K Hedlund ◽  
Ashley A Ellsworth ◽  
...  

Visible-light irradiation of phthalimide esters in the presence of the photosensitizer [Ru(bpy)3]2+ and the stoichiometric reducing agent benzyl nicotinamide results in the formation of alkyl radicals under mild conditions. This approach to radical generation has proven useful for the synthesis of small organic molecules. Herein, we demonstrate for the first time the visible-light photosensitized deposition of robust alkyl thin films on Au surfaces using phthalimide esters as the alkyl radical precursors. In particular, we combine visible-light photosensitization with particle lithography to produce nanostructured thin films, the thickness of which can be measured easily using AFM cursor profiles. Analysis with AFM demonstrated that the films are robust and resistant to mechanical force while contact angle goniometry suggests a multilayered and disordered film structure. Analysis with IRRAS, XPS, and TOF SIMS provides further insights.


2012 ◽  
Vol 51 (32) ◽  
pp. 8050-8053 ◽  
Author(s):  
Shunyou Cai ◽  
Xinyang Zhao ◽  
Xinbo Wang ◽  
Qisong Liu ◽  
Zigang Li ◽  
...  

ChemInform ◽  
2013 ◽  
Vol 44 (29) ◽  
pp. no-no
Author(s):  
Shaoqun Zhu ◽  
Arindam Das ◽  
Lan Bui ◽  
Hanjun Zhou ◽  
Dennis P. Curran ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document